61. Obstetric Ultrasound A Comprehensive Guide To Ultrasound Scans Comprehensive guide to Obstetric/ prenatal ultrasound. Covers all aspects of sonography in pregnancy Category Science Technology Ultrasound Medical Imaging ObGyn...... include hydrocephalus, anencephaly, myelomeningocoele, achondroplasia and other dwarfism,spina bifida conditions such as a) confirmation of intrauterine death http://www.ob-ultrasound.net/

A Comprehensive Guide Rated among the top 5% of all Internet sites by Lycos in 1995 And ranked first on Google for the keyword " Ultrasound" In association with Amazon.com What are Obstetric Ultrasound Scans? Obstetric Ultrasound is the use of ultrasound scans in pregnancy. Since its introduction in the late 1950’s ultrasonography has become a very useful diagnostic tool in Obstetrics. Currently used equipments are known as real-time scanners, with which a continous picture of the moving fetus can be depicted on a monitor screen. Very high frequency sound waves of between 3.5 to 7.0 megahertz (i.e. 3.5 to 7 million cycles per second) are generally used for this purpose. They are emitted from a transducer which is placed in contact with the maternal abdomen, and is moved to "look at" (likened to a light shined from a torch) any particular content of the uterus. Repetitive arrays of ultrasound beams scan the fetus in thin slices and are reflected back onto the same transducer. The information obtained from different reflections are recomposed back into a picture on the monitor screen (a sonogram, or ultrasonogram). Movements such as fetal heart beat and malformations in the feus can be assessed and measurements can be made accurately on the images displayed on the screen. Such measurements form the cornerstone in the assessment of gestational age, size and growth in the fetus.

62. Healthlink Template Factor beta Receptor','Nerve Growth Factor','beta Nerve Growth Factor','Cell Growth','GrowthHormone Deficiency dwarfism','intrauterine Growth Retardation http://healthlink.mcw.edu/search/text-search-fulllist.php?growth

63. Teleconference 08/08/02, Multiple Medical Complications in 24 Week Twins. 07/25/02, RightEctopic Twin with intrauterine Pregnancy. 0923-99, Thanatotrophic dwarfism. http://www.uams.edu/obgyn/obstetrc/teleconf.htm

High Risk OB Teleconference The High Risk OB Teleconference is held at 7:00 a.m. each Thursday. SPRING BREAK! - CANCELED Idiopathic Cyanosis of Lower Extremities Postpartum Venous Sinus Thrombosis Mechanical Valve Complicating Pregnancy First Trimester Adnexal Mass Group B Strep Prophylaxis in Pregnancy Isoimmunization in Pregnancy Canceled due to inclement weather Septic Abortion Preterm PROM Placenta Accreta HELLP Syndrome UTI in Pregnancy Antepartum Fetal Surveillance Pica in Pregnancy Management of Hyperemesis Thromboembolism in Pregnancy Revised CDC Guidelines for Prevention of Perinatal GBS Disease Gestational HTN Cervical Incompetence Fetal Urethral Obstruction Sickle Cell Disease in Pregnancy Velamentous Cord Insertion in an Intrauterine Growth Restricted Fetus Complete Placenta Previa Newborn with Undetected Myelomeningocele Tylenol Overdose in Pregnancy HSV in Pregnancy Management Multiple Medical Complications in 24 Week Twins Right Ectopic Twin with Intrauterine Pregnancy Premature Rupture of Membranes Remote from Term Septic Abortion Postop Sepsis, S/P C-Section

64. Birth Disorder Information Directory - P List of Sites. Primordial dwarfism See Growth Hormone Deficiency. Pseudotorch Syndrome(intrauterine InfectionLike Syndrome with Microcephaly, Intracranial http://www.bdid.com/defectp.htm

HOME P P-4 Deletion Syndrome A nationally recognized not-for-profit pre-school and therapeutic center for children with and without developmental delays ages 18 months to five years p47-PHOX, Deficiency of See Granulomatous Disease, Chronic, Autosomal Cytochrome-b-Positive Form, Type I p67-PHOX, Deficiency of See Granulomatous Disease, Chronic, Autosomal Cytochrome-b-Positive Form, Type II Pachydermopreiostosis (Hypertrophic Osteoarthropathy, Primary or Idiopathic) PACHYDERMOPERIOSTOSIS; PDP Pachyonychia Congenita See Jadassohn Lewandowsky Syndrome Pagod Syndrome See Kennerknecht Sorgo Oberhoffer Syndrome Pagon Bird Detter Syndrome (Anemia Sideroblastic Spinocerebellar Ataxia) Anemia sideroblastic spinocerebellar ataxia ANEMIA, SIDEROBLASTIC, AND SPINOCEREBELLAR ATAXIA; ASAT Pagon Syndrome See Walker Warburg Syndrome Pallister Syndrome See Schinzel Syndrome Pallister Hall Syndrome (Hypothalamic Hamartoblastoma, Hypopituitarism, Imperperforate Anus, and Postaxial Polydactyly) Pallister Hall syndrome:early diagnosis and natural history PALLISTER-HALL SYNDROME; PHS Also see McKusick Kaufman Syndrome Pallister Killian Syndrome V-KI-RAS2 KIRSTEN RAT SARCOMA 2 VIRAL ONCOGENE HOMOLOG; KRAS2

65. UCSD Musculoskeletal Radiology 1726 Menkes (kinky hair) syndrome. .1727 intrauterine growth retardation (dwarfism),nonspecific. .1728 Fetal alcohol syndrome, fetal Dilantin syndrome. http://medicine.ucsd.edu/bonepit/ACR film library/Pathology index.htm

UCSD Musculoskeletal Radiology bonepit.com Pathology Index .1 NORMAL ROUTINE PLAIN FILM exclude. normal variant (.13) .12 SPECIAL TECHNIQUE, PROCEDURE, PROJECTION Digital radiographic techniques, tomography, MR, nuclear medicine .1211 Computed tomography .12111 Unenhanced .12112 Enhanced with intravenous drip or bolus .12113 Dynamic enhanced technique .12114 Delayed scanning following enhancement (e.g., for detection of liver lesions) .12115 Spiral scanning .12116 CT angiography .12117 Three-dimensional reconstruction .12118 High-resolution technique .12119 Other, including serial enhancement studies (e.g., for diagnosis of hemangioma) .1214 Magnetic resonance (MR) .12141 Morphologic magnetic resonance imaging .121411 Spin echo .121412 Gradient echo .121413 Inversion recovery .121414 Chemical shift imaging .121415 Specific resonance suppressed include: fat suppression, water suppression .121416 High-speed imaging include: echo planar .121417 Magnetization transfer .121419 Other .12142 MR angiography (morphological vascular imaging) .12143 Contrast-enhanced studies, trace studies

66. Growth Failure From Pediatrics / Endocrinology Psychosocial dwarfism. Chromosomal abnormalities In particular, Turner syndrome(45,X Target tissue defects. intrauterine growth retardation The category of http://author.emedicine.com/PED/topic902.htm

eMedicine Journal Pediatrics Endocrinology Growth Failure Synonyms, Key Words, and Related Terms: slow growth velocity, short stature, growth hormone, GH Author Information Introduction Clinical Differentials ... Bibliography AUTHOR INFORMATION Section 1 of 11 Authored by Stephen Kemp, MD, PhD , Chief of Endocrinology, Professor, Department of Pediatrics, Section of Pediatric Endocrinology, University of Arkansas and Arkansas Children's Hospital Coauthored by Neslihan Güngör, MD , Instructor, Department of Pediatrics, Section of Endocrinology, Children's Hospital of Pittsburgh and University of Pittsburgh Stephen Kemp, MD, PhD, is a member of the following medical societies: American Academy of Pediatrics American Association of Clinical Endocrinologists American Pediatric Society Endocrine Society ... Southern Medical Association , and Southern Society for Pediatric Research Edited by Thomas A Wilson, MD , Director of Pediatric Endocrinology, Clinical Associate Professor, Department of Pediatrics, State University of New York at Stony Brook; Mary L Windle, PharmD

67. Wolf-Hirschhorn Syndrome From Pediatrics / Genetics And Metabolic Disease Major anomalies intrauterine growth retardation, microcephaly, cleft palate, corpuscallosum 210600) - Also known as bird-headed dwarfism or microcephalic http://author.emedicine.com/ped/topic2446.htm

eMedicine Journal Pediatrics Genetics And Metabolic Disease Wolf-Hirschhorn Syndrome Synonyms, Key Words, and Related Terms: chromosome 4p deletion syndrome, monosomy 4p syndrome, Wolf syndrome, Pitt-Rogers-Danks syndrome Author Information Introduction Clinical Differentials ... Bibliography AUTHOR INFORMATION Section 1 of 12 Authored by Harold Chen, MD, MS, FAAP, FACMG , Chief, Professor, Department of Pediatrics, Section of Perinatal Genetics, Louisiana State University Medical Center Harold Chen, MD, MS, FAAP, FACMG, is a member of the following medical societies: American Academy of Pediatrics American College of Medical Genetics American Medical Association American Society of Human Genetics , and Teratology Society Edited by Erawati Bawle, MD, FAAP, FACMG , Director, Division of Genetic and Metabolic Diseases, Children's Hospital of Michigan; Clinical Professor, Department of Pediatrics, Wayne State University School of Medicine; Robert Konop, PharmD , Clinical Assistant Professor, Department of Pharmacy, Section of Clinical Pharmacology, University of Minnesota; Robert Anthony Saul, MD

68. Zinc Deficiency And Development in patients with the syndrome of anemia, hepatosplenomegaly, dwarfism, and hypogonadism. SimmerK, Thompson R. Maternal zinc and intrauterine growth retardation http://www.iza.com/zhe_org/Articles/Art-02.htm

Zinc deficiency and development Harold H Sandstead, MD The University of Texas Medical Branch Galveston, TX USA 77555-1109 e-mail: hsandste@UTMB.edu In 1961 Prasad, Halsted and Nadimi (1) reported a syndrome of iron deficiency anemia, stunting, hypogonadism, and hepatosplenomegaly in Iranian farmers.They speculated that zinc deficiency was the cause of the stunting and delayed development. This was counter to the existing paradigm that held human zinc deficiency was highly unlikely because zinc is ubiquitous. Subsequent research in Egypt (2-6), Iran (7-10) confirmed their hypothesis, and with data from experiments in animals (11, 12) provided the basis for the hypothesis that maternal zinc deficiency contributes to the high prevalence of teratology in the region (13). The common causes of zinc deficiency are low dietary intakes and low bioavailability. Red meat is the best common source of bioavailable zinc (98,99). Therefore individuals who do not consume this food on a regular basis are at risk of zinc deficiency, just as they are of iron deficiency (100, 101). In addition similar factors affect the bioavailabilty of zinc (7, 102-111) and iron (112-114). Therefore it seemed likely that dietary zinc and iron deficiencies might be associated.

69. PIVOT 99 FETAL HYDROPS. HORMONAL IMBALANCE. HYPOLASTIC LUNG SYNDROME. intrauterine FETAL DEMISE.MULTICYSTIC (POLYCYSTIC KIDNEYS). DILATED CARDIOMYOPATHY. dwarfism. ECLAMPSIA. http://www.hygeia.org/pivot99.htm

REGISTERED DIAGNOSES January, 1996-February, 2003 TOTAL REGISTERED USERS 22,513 BLIGHTED OVUM / MISCARRIAGE CORD ACCIDENT INCOMPETANT CERVIX ABRUPTIO PLACENTA ECTOPIC PREGNANCY TRISOMY 18 PROM EXTREME PREMATURITY ALVEOLAR CAPILLARY DYSPLASIA CONGENITAL HEART DISEASE MOLAR PREGNANCY ANENCEPHALY TRISOMY 21 - DOWN SYNDROME ASPHIXIA ANTIPHOSPHOLIPID ANTIBODY SYNDROME MULTIPLE GESTATION TWIN TO TWIN TRANSFUSION SYNDROME INFECTION/SEPSIS SEVERE TOXEMIA TRISOMY 13 HYPOPLASTIC LEFT HEART SYNDROME SIDS NEURAL TUBE DEFECT STILLBIRTH TURNER'S SYNDROME IUGR MULTIPLE CONGENITAL ANOMALIES RECURRENT MISCARRIAGE CHROMOSOME TRIPLOIDY DIAPHRAMATIC HERNIA FETAL DEMISE GROUP B STREP SEPSIS DIABETES HYDROCEPHALY MECONIUM ASPIRATION SYNDROME POTTER'S SYNDROME CHORIOAMNIONITIS RDS VANISHING TWIN TRIPLODY VELAMENTOUS CORD INSERTION MENNINGITIS TRUE KNOT IN CORD CHROMOSOME TRIPLOIDY MULTIPLE LOSSES PARTIAL MOLAR PREGNANCY RENAL AGENESIS TRISOMY-OTHER TRISOMY-OTHER CONGENITAL ANOMALIES INTRAVENTRICULAR HEMMORAGE NEC FIFTH'S DISEASE/PARVO VIRUS VATER SYNDROME ALVEOLAR CAPILLARY DYSPLASIA CHROMOSOME TRIPLOIDY CYSTIC HYGROMA HYDROPS FETALIS IATROGENIC POTTER'SSYNDROME SPONTANEUS ABORTION SPINA BIFIDA BLOOD CLOT IN CORD HOLOPROSENCEPHALY LOSS OF 1 TWIN LUPUS SYNDROME NON-IMMUNE FETAL HYDROPS OMPHALOCELE TRISOMY-OTHER VASA PRAEVIA CHROMOSOMAL ABNORMALITY FIBROIDS /LEIOMYOMATA POTTER'S SYNDROME TWIN PREGNANCY CORPUS LUTEUM DEFICIENCY NEONATAL INFECTION POTTER'SSYNDROME DOWN SYNDROME FETAL HYDROPS HORMONAL IMBALANCE HYPOLASTIC LUNG SYNDROME INTRAUTERINE FETAL DEMISE MULTICYSTIC (POLYCYSTIC KIDNEYS)

70. Germplasm PURIFICATION AND CHARACTERIZATION OF intrauterine FOLATE BINDING PROTEINS FROM SWINE; INBRAHMAN FEMALES; A NOVEL PHENOTYPE FOR LARON dwarfism IN MINIATURE BOS http://www.nal.usda.gov/ttic/tektran/categoryV3/Germplasm.html

TEKTRAN Germplasm CRITICAL TRANSCRIPTION ELEMENTS WITH 1 KB OF THE WHEY ACIDIC PROTEIN GENE PROMOTER ARE ONLY ACTIVE IN THE PRESENCE OF A MATRIX ATTACHMENT REGION. ASSESSMENT OF PORCINE SPERM VIABILITY AND EMBRYO DEVELOPMENT IN GILTS INSEMINATED WITH SYBR-14 STAINED SPERM APPEARANCE OF INSULIN-LIKE GROWTH FACTOR (IGF) MRNA IN THE LIVER AND PYLORIC CAECA OF A TELEOST IN RESPONSE TO EXOGENOUS GROWTH HORMONE GROWTH HORMONE MAINTAINS BONE DENSITY AND CIRCULATING OSTEOCALCIN LEVELS IN HYPOPHYSECTOMIZED RATS SUBJECTED TO SIMULATED WEIGHTLESSNESS ... PUBERTY IN HEIFERS RAISED IN THE SUBTROPICS AS INFLUENCED BY BREED TYPE, LEVEL OF WINTER SUPPLEMENTATION, AND SUMMER GRAZING SYSTEM

71. Genetic Diseases Of The Epidermis And Its Appendages syndrome with abnormalities of placentation, severe intrauterine growth retardation ICHTHYOSIS,MENTAL RETARDATION, dwarfism, AND RENAL IMPAIRMENT, 242530, AR, In http://www.tigem.it/skin/

GENETIC DISEASE NAME OMIM CHROMOSOME LOCALIZATION GENE GENETICS ANIMAL MODEL FEATURES BULLOUS ERYTHRODERMA ICHTHYOSIFORMIS CONGENITA, BULLOUS ICHTHYOSIFORM ERYTHRODERMA, EPIDERMOLYTIC HYPERKERATOSIS EHK AD 1:300000 Widespread bullous disease at birth. Erythematous, blister hyperkeratosis. SKIN PEELING SYNDROME, FAMILIAL CONTINUOUS, KERATOLYSIS EXFOLIATIVA CONGENITA AR, very rare Type A: asymptomatic peeling Type B: erythema and pruritus, separation between stratum corneum and granulosum. Sometime short stature HARLEQUIN FETUS AR, rare ichq chrm 19 Thick plates of scales ectropion and eclabium, lethal. Male with harlequin ichthyosis with a de novo deletion of the long arm of chromosome 18; the karyotype was 46,XY,del(18)(q21.3) ICHTHYOSIS BULLOSA OF SIEMENS, ICHTHYOSIS EXFOLIATIVA IBS AD, rare May present erythema and blistering. In later weeks, large, dark gray hyperkeratoses predominantly on the arms and legs ICHTHYOSIS HYSTRIX, CURTH-MACKLIN TYPE IHCM KRT1 (1 report 2001) AD, rare Plaques and spiny hyperkeratosis, erythroderma may be present at birth. defect of tonofibrils, excluded linkage with cluster of keratin genes on 12q and 17q, however one report mutation in a keratin gene (KRT1) (JID 2001) ICHTHYOSIS HYSTRIX GRAVIOR, LAMBERT TYPE ICHTHYOSIS, PORCUPINE MAN

72. Kprones BLO10002 growth dwarfism intrauterine growth retardation; birth weightbelow 2.3 kg; mean length 44 cm; adult length 145 cm. skin http://www.infobiogen.fr/services/chromcancer/Kprones/BLO10002.html

73. CancerGene ERCC6 GROWTH Other intrauterine growth retardation Low birth weight Markedfailure to thrive Postnatal growth retardation Cachectic dwarfism. http://caroll.vjf.cnrs.fr/cancergene/CG945.html

Infobiogen Search CancerGene CancerGene Homepage Search CancerGene Citations CancerGene Card Symbol Aliases CSB Name excision repair cross-complementing rodent repair deficiency, complementation group 6; Rad26 (yeast) homolog Locus OMIM GDB SwissProt LocusLink Atlas of Genetics and Cytogenetics in Oncology and Haematology : CSB Class REPAIR Keywords transcription-coupled repair (TCR) Diseases Cockayne Syndrome; Dwarfism; Neurodegenerative Diseases; Photosensitivity Disorders Note COCKAYNE SYNDROME, TYPE B, INCLUDED; CSB, INCLUDED ( OMIM:133540 See also OMIM:216400 COCKAYNE SYNDROME, TYPE I; CKN1 (COCKAYNE SYNDROME, TYPE A; CSA). Selected MEDLINE References: [Link to NCBI] [Link to CancerGene Citation Database] Recent Articles : Lee SK;Yu SL;Prakash L;Prakash S Requirement of yeast RAD2, a homolog of human XPG gene, for efficient RNA polymerase II transcription. implications for Cockayne syndrome. Cell 2002 Jun 28;109(7):823-34. Yu A;Fan HY;Liao D;Bailey AD;Weiner AM Activation of p53 or loss of the Cockayne syndrome group B repair protein causes metaphase fragility of human U1, U2, and 5S genes. Mol Cell 2000 May;5(5):801-10

74. Malnutrition Worldwide Estimated incidence of intrauterine growth retardation as a proportion mutism, squint,spastic diplegia, mental retardation, dwarfism, stillbirth, congenital http://www.mikeschoice.com/reports/malnutrition_worldwide.htm

Malnutrition Worldwide Source: World Health Organization The spectrum of malnutrition Malnutrition throughout the lifespan Reporting on Global Malnutrition: A WHO/NUT responsibility Intrauterine growth retardation and maternal malnutrition ... Diet and Cancer The Spectrum of Malnutrition TOP Intra-uterine growth retardation Protein-energy malnutrition Iodine deficiency disorders Vitamin A deficiency Iron-deficiency anaemia Obesity and other diet-related non-communicable diseases A range of other specific nutritional deficiency diseases often related to distinct population groups, including: folate deficiency zinc deficiency calcium deficiency and osteoporosis beriberi, pellagra, scurvy selenium deficiencies Malnutrition thus covers a broad spectrum of ills, including undernutrition, specific nutrient deficiencies, and overnutrition; and it kills, maims, retards, cripples, blinds, and impairs human development on a truly massive scale worldwide. Despite significant improvements in world food supplies, health conditions, and availability of educational and social services, because of the fundamental role nutrition plays in attaining and preserving health, no population escapes malnutrition's grasp. All countries have significant population groups with some form of debilitating malnutrition. Its consequences are of enormous significance, even in terms of mortality alone. In the developing world in 1995, of the estimated 10.4 million deaths among children under 5 years of age, protein-energy malnutrition was associated and causative factor in 5.1 million of these deaths (ie 49%).

75. Clinical Case : Hydrops And Congenital Anomalies 17 weeks of gestation because of hydrops with intrauterine growth retardation IUGR,ie microcephalic dwarfism, dysmorphic facies and hypoplasia of the fibula http://www.hydropsfetalis.org/Clinical_case.html

Home About hydrops fetalis About us Other links CLINICAL CASE FRANÇAIS Miscarriage (9 weeks) Clinical synopsis Thick placenta with many blood clots Umbilical cord too long by 7 cm (no placental pathology was investigated) Microcephaly or rather the weight of brain and the cranium were normal for 14-15 weeks. Extensive autolysis of the brain should be noted. Triangular long face : bird-headed appearance Receding forehead Hypoplastic eyes with hypertelorism and microphthalmia (according to the pathologist) Narrow-shaped and downslanting or antimongoloid slant of palpebral fissures (as shown on pictures) Microtia with malformed and low-set ears (not rimmed), hypoplasia of lobes Protrusion of the nose (very prominent and pointed) Important micrognathia and retrognathia Short neck with oedema Tapering fingers and toes with hypoplastic nails (according to the pathologist) Abnormal space between the two big toes and the second toes (as shown on pictures) Absence of epiphyseal ossification at the phalanges : clinodactyly, camptodactyly ? Legs bone asymmetry : absence or hypoplasia of fibula on the right-hand side Micropenis (hypoplastic testes in pelvis were not examined under a microscope) but the "micropenis" may be normal for a fetus whose weight was 67 grammes...

76. Micropenis Indications, causes, and treatment.Category Health Men s Health Conditions and Diseases Microphallus...... Vanishing testis syndrome – intrauterine torsion; bilateral loss resultsin micropenis. Robinow syndrome mesomelic dwarfism, dental anomalies. http://www.kids-urology.com/micropenis.html

Micropenis Description: Epidemiology Statistical definition based on stretched penile length Incidence – Statistically, occurs in 0.6% of population Normal newborn penis is at least 1.9 cm long The term micropenis should not be used with other abnormalities of the penis, e.g., hypospadias Environmental factors - none Genetics – there is no genetic determinant for micropenis, but some genetic syndromes are associated with it Chromosomes – abnormal number, e.g., Klinefelter and Down syndromes Genes – genetic mutation, e.g., androgen insensitivity ("Testicular Feminization") Signs and Symptoms Signs - Small penis Symptoms - n one unless part of a syndrome Pathology/Pathophysiology Penile development includes androgen dependent and independent growth Majority of development depends on secretion of androgens First 3 months of gestation Maternal HCG causes fetal testis Leydig cells to produce testosterone Testosterone converted to dihydrotestosterone in genital tubercle by 5a-reductase type 2 Penis and urethra become completely formed during first trimester Fourth month of gestation onward Fetal hypothalamus and pituitary drive testosterone production by testi s Micropenis is generally due to inadequate testosterone stimulation during 2 nd and 3 rd trimester of gestation Additional growth at puberty, ages 11-18, due to increase in serum testosterone to adult levels

77. Malattie Rare E Genetiche Lettera "D" dwarfism, Deformity with Mesomelic/LeriWeil Dyschondrosteosis/Leri-Weil Syndrome/Leri-Weill Disease/Mesomelic dwarfism-Madelung Deformity http://utenti.tripod.it/fmfpc/D.htm

HOME FORUM Site Map / Mappa del sito FMFPC's International Guest/Book ... E-mail Dal 22 Marzo 2003 il server Lycos, che ospita le pagine FMFPC, subirà un *fermo tecnico*. Le pagine resteranno accessibili ma non verranno aggiornate per circa una settimana. - Tutti i servizi di FMFPC continueranno a funzionare. - È ora possibile accedere al sito anche attraverso l'indirizzo alternativo di FMFPC (sito mirror) all'URL http://digilander.libero.it/fmfpc/portale.htm ultimi aggiornamenti del sito Elenco malattie rare e genetiche "lettera D" © FMFPC è un sito ideato, realizzato ed aggiornato da un malato di FMF (Febbre Mediterranea Familiare) © FMFPC is a site conceived, realized and updated by a patient of FMF (Familial Mediterranean Fever) aggiornamento 27 febbraio, 2003 Cerca nel menu aree FMFPC AREE FMFPC Malattie Rare Febbre Mediterranea Familiare Laboratori Diagnosi Genetica Associazioni Malati Disabilità/Handicap Categorie Medicina (Directory) Ricerche WEB (Medicina) FMFPC è partner AidWeb.org Cerca nel sito / Search in this site I contatti fino ad oggi possibili con FMFPC: Cerca in questa pagina / Search in this page con i tasti / with the keys Ctrl+F A B C - D - E F G H ... legenda D Da Silva Sindrome di Corpus callosum, Agenesis of/ACC

78. Dwarfism - Short Stature Psychosocial Issues of Growth Delayed Children, Transition to Adult, IntrauterineGrowth Retardation Supports research in causes and treatment of dwarfism. http://www.kumc.edu/gec/support/dwarfism.html

Dwarfism / Short Stature (Skeletal Dysplasias, Achondroplasia, Jeune Syndrome constitutional delay , other conditions) Organizations Clinics International Specific Syndromes ... Little People of America (LPA) , Inc. P.O. Box 745, Lubbock, TX 79408 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 Phone: (800) 451-6434 or (703) 883-1773 Fax: (703) 883-1776 Supports basic clinical research pertaining to growth disorders. Disseminates information. Encourages development of local parent support groups. Oversees a grant research program

79. NEJM -- Laron Dwarfism And Mutations Of The Growth Hormone-receptor Gene We conclude that Laron dwarfism is due to abnormalities in the gene IntrauterineGrowth Retardation and Postnatal Growth Failure Associated with Deletion of http://content.nejm.org/cgi/content/short/321/15/989

HOME SEARCH CURRENT ISSUE PAST ISSUES ... HELP Volume 321:989-995 October 12, 1989 Number 15 Next Laron dwarfism and mutations of the growth hormone-receptor gene S Amselem, P Duquesnoy, O Attree, G Novelli, S Bousnina, MC Postel-Vinay, and M Goossens Table of Contents Find Similar Articles in the Journal Notify a friend about this article Add to Personal Archive ... Related Articles in Medline Articles in Medline by Author: Amselem, S. Goossens, M. Medline Citation Abstract Source Information Service de Biochimie and INSERM, C.H.U. Henri Mondor, Creteil, France. This article has been cited by other articles: Kopchick, J. J., Parkinson, C., Stevens, E. C., Trainer, P. J. (2002). Growth Hormone Receptor Antagonists: Discovery, Development, and Use in Patients with Acromegaly. Endocr Rev [Abstract] [Full Text] Bachelot, A., Monget, P., Imbert-Bollore, P., Coshigano, K., Kopchick, J. J., Kelly, P. A., Binart, N. (2002). Growth Hormone Is Required for Ovarian Follicular Growth. Endocrinology [Abstract] [Full Text] Laron, Z (2001). Insulin-like growth factor 1 (IGF-1): a growth hormone. Mol Pathol [Abstract] [Full Text] D'Andrea, A. D. (1994). Cytokine Receptors in Congenital Hematopoietic Disease.

80. Acromesomelic Dysplasia Hunter-Thompson Type can be also suspected by the observation of intrauterine growth retardation and Acromesomelicdwarfism description of a patient and comparison with previously http://orphanet.infobiogen.fr/data/patho/uk-hunter.html

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