21. 1Up Health > Health Links Directory >Conditions And Diseases:Genetic Disorders:D A syndrome of intrauterine dwarfism, short stature, mental retardation,sparse hair, eczema, and characteristic facies. The phenotype http://www.1uphealth.com/links/desc-534.html

Home Contact Us Privacy Caring For Your Well Being Alternative Medicine Clinical Trials Health News Poisons ... Health Topics A-Z Search 1Up Health Health Directory Addictions Alternative Animal ... Weight Loss By Demography Child Health Teen Health Men's Health Women's Health ... Health Directory A syndrome of intrauterine dwarfism, short stature, mental retardation, sparse hair, eczema, and characteristic facies. The phenotype varies from normal growth and head circumference with mild psychomotor retardation and lack of eczema to severe growth and mental retardation, microcephaly, behavioral problems, aplastic anemia, immunological disorders, neoplasms, and eczema Some features of this syndrome are similar to those in Bloom and fetal alcohol syndromes. Help build the largest human-edited directory on the web. Submit a Site Open Directory Project Become an Editor Parts of the directory made available on 1UpHealth have been modified. External Web site links provided on this site are meant for convenience and for informational purposes only; they do not constitute an endorsement. Search: The information provided herein should not be used during any medical emergency or for the diagnosis or treatment of any medical condition. A licensed physician should be consulted for diagnosis and treatment of any and all medical conditions. Call 911 for all medical emergencies. Links to other sites are provided for information only they do not constitute endorsements of those other sites.

22. Katalog Health Conditions_and_Diseases I - Netz-Tipp. intrauterine dwarfism(*); Iritis (*); Irritable Bowel Syndrome (*); Isaacs Syndrome (*). Jetzt chatten! http://www.netz-tipp.de/kat/Health/Conditions_and_Diseases/I/

23. Conditions And Diseases: I | Treasure Coast Health intrauterine dwarfism@ (5); Iritis@ (27); Irritable Bowel Syndrome@(70); Isaacs Syndrome@ (3). Our Sponsers. Home Doctors by Specialty http://treasurecoasthealth.com/treasurecoasthealth.php/Health/Conditions_and_Dis

Find Doctors on the Treasure Coast Select Specialty Ambulatory Care Anesthesiology Cardiology Dermatology Emergency Medicine Endocrinology Family Practice Gastroenterology Hematology/Oncology Infectious Diseases Internal Medicine Maxillofacial Surgery Neonatology Nephroology Neurology Neurosurgery Obstetrics/Gynecology Ophthalmology Orthopedic Surgery Otolaryngology Pathology Pediatics Physical Medicine Plastic Surgery Podiatry Psychiatry Psychology Pulmonary Radiation Oncology Radiology Rheumatology Surgery Thoracic Surgery Urology Vascular Surgery Select City Sebastian Palm Bay Vero Beach Fort Pierce Okeechobee Port St. Lucie Jensen Beach Stuart Palm City Hobe Sound Loxahatchee MENU Home Doctor Directory Health Resources Women Only ... About Us Conditions and Diseases: I Chronic Fatigue Syndrome IgA Nephropathy Imperforate Anus Impotence ... Isaacs Syndrome Our Sponsers Home Doctors by Specialty Doctors by City Health Resources ... Contact Webmaster We subscribe to the HONcode principles Verify here.

24. Dubowitzin Oireyhtymä Kehitysvammahuollon tietopankki. intrauterine dwarfism (kohdunsisäinenkääpiökasvuisuus). Dubowitzin oireyhtymä. Dubowitzin oireyhtymä http://www.saunalahti.fi/kup/syndroma/dubowitz.htm

Kehitysvammahuollon tietopankki Intrauterine dwarfism (kohdunsisäinen kääpiökasvuisuus) Dubowitzin oireyhtymä Dubowitzin oireyhtymä on hyvin harvinainen sairaus (vuosittain syntyy koko maailmassa n. 40 lasta), jota luonnehtii kasvun hidastuminen, lyhytkokoisuus ja poikkeavat kasvonpiirteet. Oireet voivat ilmaantua jo sikiövaiheessa tai heti syntymän jälkeen. Sairastuneista puolet kehitysvammaisia Noin puolet oireyhtymään sairastuneista on kehitysvammaisia. Henkinen jälkeenjääneisyys on useimmiten lievää Dubowitzin oireyhtymän erikoispiirteitä ovat pienipäisyys, kallon saumojen ennenaikainen luutuminen, korkea otsa ja leveä nenänselkä, poikkeavat silmäkuopat, etäällä toisistaan olevat silmät ( hypertelorismi ) ja riippuluomet sekä luomirakojen ahtaus. Niinikään kasvojen, polvien ja kyynärpäiden syyhyävät punaiset ihoalueet ovat tavanomaisia. Ääni on erikoisen korkea tai käheä. Leuka on usein pienikokoinen ja nielu vajaakehittynyt. Epämuodostumia ja poikkeuksellista tulehdusalttiutta Muina oireina esiintyy mm. piilokiveksisyyttä, siittimen alahalkioita, valtimoiden poikkeavuuksia, peräaukon epämuodostumista ja lisäkilpirauhasen vajaatoimintaa. Lisäksi infektioalttius, uusiutuvat haavaiset suutulehdukset, lisääntynyt kasvainriski ja luuytimen vaurioituminen sekä valkosolujen niukkuus ovat osa taudinkuvaa.

25. DINO - Language: Englisch - Health - Conditions And Diseases - I Translate this page Cystitis Dieser Link verweist auf eine Haupt-Kategorie Intracranial Hypotension DieserLink verweist auf eine Haupt-Kategorie intrauterine dwarfism Dieser Link http://www.dino-online.de/dino_page_b59e5599eff149a938d21be50751a806.html

Suche Profi-Suche Katalog Video ... Produkte Suchen: Web-Seiten Video Audio Bilder Produkte Schon gewusst? Hier suchen Sie in 2 Milliarden Webseiten. Live-Suche: Was suchen andere Dino-Besucher? You are here: DINO Language Englisch Health ... Conditions and Diseases I I Sprache/Language Categories Chronic Fatigue Syndrome IgA Nephropathy Imperforate Anus Impotence Impulse Control Disorders Incontinence Incontinentia Pigmenti Indigestion Infections and Viruses Infertility Inflammatory Bowel Disease Influenza Insomnia Insulin Resistance Intermittent Explosive Disorder Internet Addiction Interstitial Cystitis Intracranial Hypotension Intrauterine Dwarfism Iritis Irritable Bowel Syndrome Isaacs Syndrome This site is based on the Open Directory Project (ODP) Last update: 08. Jul. 2002, 18:02:37 o'clock This categorie needs an Editor. Help build the largest human-edited directory of the web: Become an Editor Services AKTUELLE Nachrichten Topthemen Wirtschaft Deutschland Sport ... Kalender DOMAIN NOCH FREI? www. .DE .COM .NET .ORG .INFO .BIZ .TV .WS Weitersagen Seite Drucken Zum Seitenanfang Home ... Home Weitere Angebote der freenet.de AG:

26. Principles Of Pediatric Dermatology - Chapter 32 : GENODERMATOSES The hair may be sparse and prematurely gray. Diagnosis. The syndrome mustbe differentiated from others in which there is intrauterine dwarfism. http://www.drmhijazy.com/english/chapters/chapter32_2.htm

CHAPTER 32 GENODERMATOSES Contents Search Recessive epidermolysis bullosa The recessive dystrophic epidermolysis bullosa has the same cutaneous features of the dominant type. Skin manifestations Large, flaccid often-hemorrhagic bullae appear after birth or early in infancy. Mucous membrane manifestations Severe scarring of the mucous membranes of the mouth, pharynx, esophagus and the condition may be fatal. Nail dystrophy is a common complication of the recessive type of epidermolysis bullosa. Secondary bacterial infection is common and causes more complications. Fig. 256. Epidermolysis, Recessive Dystrophic Type Fig. 257. Epidermolysis Bullosa Differential Diagnosis Bullous diseases In infancy, differentiation of epidermolysis bullosa from other bullous eruptions is rarely a problem. Benign chronic bullous disease of childhood may mimic inverse types of EB since the blistering occurs around the genitalia, perineum and buttocks. However, histology of these conditions is diagnostic and the presence of linear IgA on direct immunofluorescence may help to confirm the diagnosis. Dominant bullous ichthyosiform erythroderma.

27. Vindex, De Vindplaats Van Het Nederlandse Web Resistance@ Intermittent Explosive Disorder@, Internet Addiction@ InterstitialCystitis@ Intracranial Hypotension@ intrauterine dwarfism@ Iritis@ Irritable http://www.vindex.nl/dir/Health/Conditions_and_Diseases/I

hulp contact persoonlijke instellingen voeg uw site toe ... Opties: Samenvatting 1 url per domein Sites in nieuw venster Staat uw webpagina nog niet in Vindex? Meld deze dan nu aan! Url: Emailadres: Zoek in de webgids: Terug naar het overzicht Huidige rubriek Health Conditions and Diseases I Subrubrieken Chronic Fatigue Syndrome@ IgA Nephropathy@ Imperforate Anus@ Impotence@ ... Isaacs Syndrome@ Links In deze rubriek zijn geen links gevonden... Kies een subrubriek of een verwante rubriek. Submit a Site Open Directory Project Become an Editor Powered by IBM -server IDG.nl vang.net Vragen? Opmerkingen? Suggesties?

28. Seckel's Syndrome (www.whonamedit.com) An intrauterine form of dwarfism characterized by proportional short stature, reduced circumference of the......Seckel's syndrome An intrauterine form of dwarfism. Also known as Harpers syndrome Seckel's bird head syndrome Seckel's nanism VirchowSeckel syndrome. http://www.whonamedit.com/synd.cfm/869.html

Home List categories Eponyms A-Z Biographies by country ... Contact Seckel's syndrome Also known as: Harper’s syndrome Seckel's bird head syndrome Seckel's nanism Virchow-Seckel syndrome Synonyms: Bird-headed dwarfism, birdlike face syndrome, microcephalic primordial dwarfism, nanocephalic syndrome, nanocephaly syndrome. Associated persons: Rita G. Harper Helmut Paul George Seckel Rudolf Ludwig Karl Virchow Description: An intrauterine form of dwarfism characterized by proportional short stature, reduced circumference of the cranium, a characteristic bill-like protrusion of the central area of the face with microcephaly, prominent sometimes beaked nose, large ears, sparse hair, joint defects, clubfoot, trident hands, absence of some teeth, cloacalike malformation of genitourinary tract and rectum, mental retardation and sweet disposition. A small, simplified cerebrum resembles the chimpanzee brain (pongidoid microcephaly. There is a reduction in the number of blood cells. Both sexes affected; present at birth. Inheritance is autosomal recessive. There has been described a case in which all the features of the syndrome were present, but not the dwarfism. This could be an incomplete form or a variant of the syndrome. Seckel in 1960 described the disease picture on the basis of two cases he had studied in Chicago, as well as 13 cases of nanocephalic dwarfs reported in the literature over a 200-year period. Amongst the affected persons whom Seckel discussed was Caroline Crachami, whose skeleton now reposes in the Hunterian Museum of the Royal College of Surgeons, London. Crachami, an exhibitionist known as the "Sicilian Fairy" was 49,5 cm i height when she died in 1824 at the age of nine years.

29. Health Library - Seckel Syndrome to birth (intrauterine growth retardation) resulting in low birth weight. Growthdelays continue after birth (postnatal) resulting in short stature (dwarfism). http://health_info.nmh.org/Library/HealthGuide/IllnessConditions/topic.asp?hwid=

30. Dwarfism Principal causes of dwarfism. HARMONIC dwarfism. Familial low height. intrauterine growth defect http://www.amersham-health.com/medcyclopaedia/Volume%20VI%201/DWARFISM.html

Medcyclopaedia About Medcyclopaedia Amersham Health Search for: Type a word or a phrase. All forms of the word are searchable. Advanced search Browse entry words starting with: A B C D ... Other characters Try our Medcyclopaedia Premium Edition with added tools and functionality tailored to make your working day easier. The following tools are presently available: Expanded search *For Medical Professionals only, registration required Dwarfism, In harmonic dwarfism neuroradiological interest is focused particularly on hypopituitarism and MR imaging of the sellar region is suggested as specific anomalies may be identified. Other items of neuroradiological interest are coeliac sprue precocious puberty and Cushings syndrome , the cause of which again may reside in identifiable hypothalamic/hypophyseal pathology. In disharmonic dwarfism, he diagnosis can often be established by clinical phenotypic features. Among the causes of disharmonic dwarfism, achondroplasia presents particular features that merit neuroradiological investigation and these are discussed in their specific sections (see achondroplasia ). Table 1 presents most frequent causes in the two settings.

31. Worldbook Medical Encyclopedia > Dacryocystitis - Débridement > Dwarfism A comprehensive look at the topic dwarfism The syndrome of familial dwarfism and high plasma in subjects with intrauterine growth retardation. http://www.s-books.com/wbmedical/30879/31027/Educational_Sources1.htm

Worldbook Medical Encyclopedia Dacryocystitis - Débridement Dwarfism Dwarfism Search the Web with All Surfable Books World Book Encyclopedia 2000 World Book Medical Encyclopedia Geography History Humanities Industry and Technology Life Science Physical Science and Math Recreation Social Science Documents 1 - 6 of 6 on the subject : Dwarfism Public Educational Sources News and Magazines Encyclopedias INHERITANCE INHERITANCE Biological Significance of Sex Types of Reproduction Reproduction is a basic characteristic of all forms of life. There are two types: sexual and asexual. In sexual reproduction new individuals come about through the union of sp http://www.csupomona.edu/~biology/bio110/inherit/genes.html Gender Analysis and Economic Development in West Virginia Gender Analysis and Economic Development in West Virginia Ann M. Oberhauser, Lillian J. Waugh, and Chris Weiss Women are a vital and increasingly important part of West Virginias economy. Between 1980 and 1994, the percentage of jobs held by women http://www.polsci.wvu.edu/ipa/par/report_13_2.html

32. Dwarfism Midget Short Stature Growth Hormone Defects Skeletal Dysplasia Most Little People are born to families with NO HISTORY of dwarfism 7 Postnatalgrowth and, to a much lesser degree, intrauterine growth are critically http://ibis-birthdefects.org/start/shortsta.htm

Tips for printing Short Stature About I.B.I.S. Home Search Topics Search all contents ... "In the News" Messages... Questions/comments Report Dead Links S.O.S. - Exchange Join I.B.I.S. ... Etchings Please Explore: Support Groups Professional Associations Key Information Sources Topics include Title and Growth Hormone Defects Dwarfism Midget Nanism Skeletal Dysplasia Special Resources Short Stature Achondroplasia A Selection of Internet Sites [*] Outstanding [P] For Professionals [S] Support Groups [French] [S] Short Stature from Medline plus Health Information Medical Encyclopedia A relative term used in referring to any person that is more than two standard deviations below the average height (approximately in the shortest 5%) for a person of the same age and sex ... Short stature may be a symptom caused by a medical condition and, as many of these conditions are treatable, should be evaluated by a health care provider. Common causes: - familial short stature ... - delayed puberty ... - ... hypothyroidism ...

33. Dwarfism - Short Stature of Persons of Short Stature regroups people who have dwarfism and/or Issues of GrowthDelayed Children, Transition to Adult, intrauterine Growth Retardation http://www.kumc.edu/gec/support/skeldysp.html

Dwarfism / Short Statur e (Skeletal Dysplasias, Achondroplasia, Jeune Syndrome Organizations Clinics International ... Little People of America (LPA) , Inc. P.O. Box 745, Lubbock, TX 79408 Toll free help line: (888) LPA-2001 (24 hours daily) E-mail: LPADataBase@juno.com Web Site: www.lpaonline.org Little People of America Teen Page, Books Organization Links Types of Dwarfism and Definitions LPA Parents' Forum (not currently active, web only), Mayeux family, jmayeux@gte.net LPA Parents' Committee - Rob and Betty Jacobsen, 3010 Olympia Way, Longview, WA 98632, Voice: (360) 636-0276, BBS/fax: (360) 578-1948, E-mail: jacobsen@aone.com Frequently Asked Questions Languages: English, Spanish dwarfism.org Billy Barty Foundation, Inc. 929 W Olive Avenue, Suite C, Burbank, CA 91506 Phone: (818) 953-5410 Fax: (818) 953-7129 Web site: www.rth.org/bbf/ Educational and lobbying for individuals with dwarfism Human Growth Foundation 7777 Leesburg Pike (P.O. Box 309), Falls Church, VA 22043

34. Dwarfism HARMONIC dwarfism, Familial low height. intrauterine growth defect. hypopituitarism.Cushings syndrome. Exogenous steroid therapy. precocious puberty. http://www.amershamhealth.com/medcyclopaedia/Volume VI 1/DWARFISM.asp

Medcyclopaedia About Medcyclopaedia Amersham Health Search for: Type a word or a phrase. All forms of the word are searchable. Advanced search Browse entry words starting with: A B C D ... Other characters Try our Medcyclopaedia Premium Edition with added tools and functionality tailored to make your working day easier. The following tools are presently available: Expanded search *For Medical Professionals only, registration required Dwarfism, In harmonic dwarfism neuroradiological interest is focused particularly on hypopituitarism and MR imaging of the sellar region is suggested as specific anomalies may be identified. Other items of neuroradiological interest are coeliac sprue precocious puberty and Cushings syndrome , the cause of which again may reside in identifiable hypothalamic/hypophyseal pathology. In disharmonic dwarfism, he diagnosis can often be established by clinical phenotypic features. Among the causes of disharmonic dwarfism, achondroplasia presents particular features that merit neuroradiological investigation and these are discussed in their specific sections (see achondroplasia ). Table 1 presents most frequent causes in the two settings.

35. Dwarfism Inborn errors of metabolism. intrauterine infections. Systemic inflammatorydiseases. Renal tubular disorders. Psychosocial dwarfism. Neurologic disorders. http://www.amershamhealth.com/medcyclopaedia/Volume III 1/dwarfism.html

Medcyclopaedia About Medcyclopaedia Amersham Health Search for: Type a word or a phrase. All forms of the word are searchable. Advanced search Browse entry words starting with: A B C D ... Other characters Try our Medcyclopaedia Premium Edition with added tools and functionality tailored to make your working day easier. The following tools are presently available: Expanded search *For Medical Professionals only, registration required Dwarfism, smallness of stature from various causes (Table 1). For a general description, see dwarfism Dwarfism, Table 1. Some causes of short stature. Endocrine disorders Hypopituitarism Hypothyroidism Diabetes mellitus Hypercortisolism Congenital adrenal hyperplasia Deficient somatomedin production (Laron dwarfism) Chronic disorders of major organ systems Chronic renal disease Congenital heart disease Juvenile chronic arthritis Sickle cell anaemia Malabsorption syndromes Skeletal disorders Achondroplasia Osteochondrodysplasia Pseudohypoparathyroidism and pseudopseudohypoparathyroidism Rickets Chromosomal aberrations Gonadal dysgenesis Trisomy conditions Miscellaneous disorders Malnutrition Familial short stature Inborn errors of metabolism Intrauterine infections Systemic inflammatory diseases Renal tubular disorders Psychosocial dwarfism Neurologic disorders Different types of dwarfism are described more fully under the names of specific dysplasias osteochondrodysplasias and Hypopituitarism DR The Encyclopaedia of Medical Imaging Volume III:1 Welcome to Medcyclopaedia.

36. Hans-Rudolf Wiedemann (www.whonamedit.com) Rautenstrauch syndrome A syndrome characterised by intrauterine growth retardation,low mainly by pseudorachitic long bone metaphyses and micromelic dwarfism. http://www.whonamedit.com/doctor.cfm/1001.html

Home List categories Eponyms A-Z Biographies by country ... Contact Hans-Rudolf Wiedemann German paediatrician, born February 16, 1915, Bremen. Associated eponyms: Beckwith-Wiedemann syndrome A syndrome comprising gigantism, macroglossia and umbilical abnormalities in newborn, enlarged liver and spleen, hyperplasia of the kidney, congenital abnormalities of the urinary tract, slight microcephaly, clonic seizures, often omphalocele. Genee-Wiedemann syndrome or disease An extremely rare genetic multiple congenital anomalies syndrome. Maroteaux-Spranger-Wiedemann syndrome A disturbance evident at birth characterized in childhood by dwarfism with normal body length and disproportionately long trunk, especially thorax, and short limbs, narrow chest, prominent joints, limited joint movement. Proteus' syndrome A congenital syndrome characterised by a variety of abnormalities Spranger-Wiedemann syndrome A syndrome of disproportionate dwarfism, short spine, brevicollis, barrel chest, pectus carinatum, genu valgum, flat face, myopia, malar hypoplasia, kyphoscoliosis, and limited joint mobility. Stüve-Wiedemann syndrome A rare disorder characterized by bowing of the long bones, short stature, camptodactyly, respiratory distress, episodes of unexplained hyperthermia, growth and mental retardation.

37. ORPHANET® : Base De Données Sur Les Maladies Rares Et Les Médicaments Orpheli Association of Proportionate dwarfism of prenatal onset - Characteristic dysmorphic Seckelsyndrome is characterized by - intrauterine growth retardation http://orphanet.infobiogen.fr/data/patho/GB/uk-seckel.html

Seckel syndrome Creation date: July 2001 Disease name and synonyms Prevalence Diagnosis criteria/Definition Clinical description ... References Disease name and synonyms Seckel syndrome Seckel dwarfism Bird-headed dwarfism Nanocephalic dwarfism Microcephalic primordial dwarfism 1 Prevalence It is unknown. More than 100 cases have been reported to date. Diagnosis criteria/Definition Association of: - Proportionate dwarfism of prenatal onset - Characteristic dysmorphic features including severe microcephaly and a bird-headed like appearance - Mental retardation - Autosomal recessive inheritance Clinical description Seckel syndrome is characterized by: - Intrauterine growth retardation (average birth weight 1540g); - Severe proportionately short stature with severe microcephaly (Mean postnatal growth retardation is -7 SD with a range from -5 to -13 SD / Mean OFC is -9 SD with a range from -4 to -14SD); - A "bird-headed" profile with receding forehead, large eyes, beak-like protrusion of the nose, narrow face, receding lower jaw, micrognathia; - Mental retardation. Half of the patients have an IQ less than 50;

38. ClinicalTrials.gov - Linking Patients To Medical Research: Results With intrauterine Growth Retardation Condition intrauterine Growth Retardation. inOsteogenesis Imperfecta Conditions dwarfism; Osteogenesis Imperfecta. 19. http://www.clinicaltrials.gov/ct/gui/action/SearchAction?term=Growth Disorders

39. Gale Encyclopedia Of Childhood And Adolescence: Dwarfism Environmental factors that influence intrauterine growth include maternal use ofdrugs The four most common causes of dwarfism in children are achondroplasia http://www.findarticles.com/g2602/0002/2602000208/p1/article.jhtml

Find Articles Home View By Subject View By Name Search Tips ... Help Search all magazines this magazine Arts/Entertain. Automotive Business/Fin. Comp./Tech. Health/Fitness Home/Family News/Society Reference/Ed. Sports for Search Tips : Use quotes to find a specific phrase, e.g. "Abe Lincoln" or "New York". Use the + sign for words that MUST be in the article, e.g. +Ford +SUV Terms related to this article: Dwarfism Buy and sell " " and millions of other items at eBay Gale Encyclopedia of Childhood and Adolescence Search this Magazine Go to Web site Print this article Email this article Page: Next Dwarfism Author/s: Term applied broadly to a number of conditions resulting in unusually short stature. While dwarfism is sometimes used to describe achondroplasia, a condition characterized by short stature and disproportionately short arms and legs, it is also used more broadly to refer to a variety of conditions resulting in unusually short stature in both children and adults. In some cases physical development may be disproportionate, as in achondroplasia, but in others the parts of the body develop proportionately. Short stature may be unaccompanied by other symptoms, or it may occur together with other problems, both physical and mental. Adult males under 5 ft (1.5 m) tall and females under 4 ft 8 in (1.4 m) are classified as short-statured. Children are considered unusually short if they fall below the third percentile of height for their age group. In 1992 there were about five million people of short stature (for their age) living in the United States, of which 40% were under the age of 21.

40. Home Organizations Medical Library Legal Gallery Registry Zwain For families with children who have Russell Silver intrauterine growth retardation. ofPersons of Short Stature regroups people who have dwarfism and/or http://www.dwarfism.org/orgs.php

Webmasters: 46 Dwarfism Related Organizations Asociacion Nacional Para Problemas de Crecimiento, Crecer c/o Cuartel de Artillería, 12 - bajo, E - 30002 Murcia Spain Phone: 34-968-34-62-18 Fax: +34 968 34 62 02 Francisco Jose Vela de Oro European Growth Federation. Chairman: Nuria de Oro Bertran Asociacion para las Deficiencias que afectan al Crecimiento y al Desarrollo (ADAC) Manuel Villalobos 41, Sevilla CP 41009 Spain Phone: (954) 35 87 86 Fax: (954) 35 87 86 Teresa Barco , President Association Belge des Personnes de Petite Taille Avenue des Grenadiers, 27, 1330 Rixensart Belgium Phone: +32 (0)2 653 99 23 José Leblanc , Secretary Little People of Belgium. We speak in three languages : French, English, and Nederland. Our first subject is achondroplasia. They also have a mirror site at http://www.geocities.com/capecanaveral/launchpad/3459 Association for Children with Russell Silver Syndrome, Inc. 22 Hoyt Street, Madison, NJ 07940 Phone: (201) 377-4531 Jodi Zwain For families with children who have Russell Silver intrauterine growth retardation. Alternate Number (313) 242-2219 Association for People of Short Stature in Sweden (APSSS) Foreningen For Kortvuxna-DHR, Enebackevagen 6, 435 42 S-Molnlycke, Sweden

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