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         Porencephaly:     more detail
  1. The Official Parent's Sourcebook On Porencephaly: A Revised And Updated Directory For The Internet Age by Icon Health Publications, 2004-02-13
  2. Porencephaly: An entry from Thomson Gale's <i>Gale Encyclopedia of Neurological Disorders</i> by Larry, PhD Gilman, 2005

21. Porencephaly
porencephaly,, Print this article, cavity in the brain resulting from focal tissuedestruction due to different causes, mainly ischaemic but also posttraumatic.
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*For Medical Professionals only, registration required Porencephaly, cavity in the brain resulting from focal tissue destruction due to different causes, mainly ischaemic but also posttraumatic. A more correct definition would be focal atrophy. In children, porencephaly is manifested by focal cavities with smooth walls and minimal surrounding glial relation following destruction of a portion of the germinal matrix before the 26th gestational week. According to some authors, this should be called agenetic porencephaly (which is frequently accompanied by anomalies of the overlying cortex) and distinguished from encephaloplastic porencephaly that develops later in the second trimester, and from encephalomalacia (see multicystic encephalomalacia encephalomalacia ), that results from late gestational, perinatal or postnatal injuries.

22. Porencephaly
only. porencephaly,, Print this article, attenuation. It may be difficultto distinguish ex vacuo dilatation of the ventricles from porencephaly.
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*For Medical Professionals only, registration required Porencephaly, term that is most frequently used to describe a smooth walled, fluid-filled cavity (a porencephalic cyst), which results from an insult to the immature fetal brain in the late second trimester. The limited capacity for astrocytic reaction at this time of development means that necrotic tissue is largely resorbed (liquefaction necrosis). This is in contrast to damage later in development which is associated with a more profound astrocytic proliferation which results in a cavity containing numerous septations and significant surrounding gliosis. These porencephalic cysts are occasionally termed encephaloclastic. On imaging studies, porencephalic cysts appear as smooth walled cavities which contain fluid of CSF characteristics on all sequences or attenuation profiles (

23. Porencephaly - Condition, Disease, Or Disorder Article
porencephaly Article relating to particular medical disease, condition,or disorder. porencephaly. What is porencephaly? porencephaly
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Porencephaly What is Porencephaly? Porencephaly is an extremely rare disorder of the central nervous system involving cysts or cavities in a cerebral hemisphere. The cysts or cavities are usually the remnants of destructive lesions, but are sometimes the result of abnormal development. The disorder can occur before or after birth. Most infants show symptoms of the disorder shortly after birth. Diagnosis is usually made before age 1. Signs may include delayed growth and development, spastic paresis (slight or incomplete paralysis), hypotonia (low muscle tone), seizures (often infantile spasms), and macrocephaly (large head) or microcephaly (small head). Individuals with porencephaly may have poor or absent speech development, epilepsy, hydrocephalus, spastic contractures (shrinkage or shortening of a muscle), and mental retardation. Is there any treatment?

24. DWS, Arachnoid Cyst, Porencephaly
Neither is MGH or MGH Neurology responsible for the content of any articles or replies.No messages are screened for content. DWS, Arachnoid Cyst, porencephaly.
http://neuro-www.mgh.harvard.edu/forum_2/GeneralNeurologyF/11.6.995.06PMDWSArach
This Web Forum is not moderated in any sense. Anyone on the Internet can post articles or reply to previously posted articles, and they may do so anonymously. Therefore, the opinions and statements made in all articles and replies do not represent the official opinions of MGH and MGH Neurology. Neither is MGH or MGH Neurology responsible for the content of any articles or replies. No messages are screened for content.
DWS, Arachnoid Cyst, Porencephaly
This article submitted by Brenda Savage on 11/6/99.
Email Address: savage@consultant.com
Looking for a detail explanation of the differences and similarities of Dandy-Walker Syndrome, Arachnoid Cyst, and Porencephaly. Please email me at savage@consultant.com There are Support Lists for each of these at http://www.onelist.com Next Article
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25. Encephaloclastic Porencephaly
Encephaloclastic porencephaly. This article submitted by Kate Honouron 7/31/98. Email Address prostreet@xtra.co.nz My daughter
http://neuro-www.mgh.harvard.edu/forum/CerebralPalsyF/7.31.987.55AMEncephaloclas
Encephaloclastic Porencephaly
This article submitted by Kate Honour on 7/31/98.
Email Address: prostreet@xtra.co.nz
My daughter was born fifteen weeks prematurly. She weighed 750grm. She was doing very well until four weeks of age when she developed a lung infection. In their wisdom the doctors involved began a very intense vigorous long chest physiotherapy program. Because there was no head support and the therapy was so vigorous my daughter received massive brain injury which has now been called Encephalcolastic Porencephaly. There were thirteen babies affected in this manner. Eight died. My daughter has cererbal palsy, epilesy, apnea, left hemipligia, autistic characteristics, and many other problems.
This is very breif but if there is any one with information on this type on injury or has any advice i would be very gratefull
This has been hushed up in NZ. Which is silly because we can not sue and have very little support and or help.
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26. 1Up Health > Health Links Directory > Conditions And Diseases: Neurological Diso
123). Sites. The CaF Directory A brief description of porencephaly alongwith a contact group for those residing in the UK. MCW Health
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A brief description of porencephaly along with a contact group for those residing in the UK. MCW Health Link An article about porencephaly, which is an extremely rare disorder of the central nervous system involving cysts or cavities in a cerebral hemisphere. National Institute of Neurological Disorders and Stroke Porencephaly information sheet compiled by NINDS. National Library of Medicine A summary about porencephaly and a list of major features. 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.

27. 1Up Health > Health Links Directory >Conditions And Diseases:Neurological Disord
1UpHealth Health Directory Conditions_and_Diseases Neurological_Disordersporencephaly porencephaly is an extremely rare disorder
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... Porencephaly Porencephaly is an extremely rare disorder of the central nervous system involving cysts or cavities in a cerebral hemisphere.
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28. Porencephaly : Meddie Health Search
MCW Health Link An article about porencephaly, which is an extremely rare disorderof the central nervous system involving cysts or cavities in a cerebral
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29. Porencephaly
Subscribe now . porencephaly. porencephaly is an extremely rare disorder of thecentral nervous system involving cysts or cavities in a cerebral hemisphere.
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Porencephaly
Porencephaly is an extremely rare disorder of the central nervous system involving cysts or cavities in a cerebral hemisphere. The cysts or cavities are usually the remnants of destructive lesions, but are sometimes the result of abnormal development. The disorder can occur before or after birth. Most infants show symptoms of the disorder shortly after birth. Diagnosis is usually made before age 1. Signs may include delayed growth and development, spastic paresis (slight or incomplete paralysis), hypotonia (low muscle tone), seizures (often infantile spasms), and macrocephaly (large head) or microcephaly (small head). Individuals with porencephaly may have poor or absent speech development, epilepsy, hydrocephalus, spastic contractures (shrinkage or shortening of a muscle), and mental retardation. Treatment may include physical therapy, medication for seizure disorders, and a shunt for hydrocephalus.

30. Dorlands Medical Dictionary
sweat pore, porus sudoriferus. taste pore, porus gustatorius. porencephalia(por·en·ce·pha·lia) (por²ensschwa-fal¢e-schwa) porencephaly.
http://www.mercksource.com/pp/us/cns/cns_hl_dorlands.jspzQzpgzEzzSzppdocszSzuszS

31. Schizencephaly And Porencephaly :
Schizencephaly and porencephaly porencephaly.
http://www.angelfire.com/nc/neurosurgery/GGSchizenc.htm
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32. Schizencephaly And Porencephaly :
Schizencephaly and porencephaly Schizencephaly. main page. more
http://www.angelfire.com/nc/neurosurgery/GGSchizenc2.htm
Schizencephaly and porencephaly : Schizencephaly main page more...

33. WebGuest - Open Directory : Health : Conditions And Diseases : Neurological Diso
123). Sites The CaF Directory A brief description of porencephalyalong with a contact group for those residing in the UK. MCW
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34. Fetal MRI: Porencephaly
home head and neck brain face spine chest abdomen genitourinary extremities.porencephaly. Postnatal imaging corresponds to the 38 week fetus above.
http://134.174.229.219/radiology/research/mri/fetalatlas/brain/porenceph/porence
Porencephaly Postnatal imaging corresponds to the 38 week fetus above.

35. Fetal MRI: Brain
Holoprosencephaly HydrancephalyHydrancephaly Megacisterna magnaMegacisterna MagnaPolymicrogyriaPolymicrogyria porencephalyporencephaly Tuberous sclerosis
http://134.174.229.219/radiology/research/mri/fetalatlas/brain/brain.html
14-16 weeks gestational age
17-18 weeks gestational age
19-20 weeks gestational age
21-22 weeks gestational age
23-24 weeks gestational age
25-26 weeks gestational age
27-28 weeks gestational age
29-30 weeks gestational age
31-32 weeks gestational age
33-34 weeks gestational age
35-36 weeks gestational age 37-38 weeks gestational age Corpus callosum/septum pellucidum Agenesis of the Corpus Callosum Agenesis of the Septi Pellucidi Anencephaly Arachnoid Cyst Arnold-Chiari Malformation Arteriovenous Malformation Cerebellar Hypoplasia Colpocephaly Dandy-Walker Variant/Malformation Encephalocele Hemorrhage Holoprosencephaly Hydrancephaly Megacisterna Magna Polymicrogyria Porencephaly Tuberous sclerosis Tumor Vein of Galen Malformation Venous Malformation Ventriculomegaly: Mild Ventriculomegaly: Moderate Ventriculomegaly: Severe

36. Searchalot Directory For Porencephaly
Related Web Sites. National Institute of Neurological Disorders andStroke porencephaly information sheet compiled by NINDS. MCW
http://www.searchalot.com/Top/Health/ConditionsandDiseases/NeurologicalDisorders
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37. Indian Pediatrics - Editorial
Unilateral porencephaly. prognosis of each type generally depends on the extentof the lesion(3). We report a case of unilateral porencephaly. Case Report.
http://www.indianpediatrics.net/may2002/may-495-497.htm
Home Past Issue About IP About IAP ... Subscription Case Reports Indian Pediatrics 2002; 39:495-497 Unilateral Porencephaly S. Bhagyabati Devi
N. Biplab Singh
Th. Bhimo Singh
M. Kulachandra Singh
Ksh. Chourjit Singh
From the Regional Institute of Medical Sciences, Imphal, India. Correspondence to: Dr. S. Bhagyabati Devi, Assistant Professor, Department of Medicine, Regional Institute of Medical Sciences, Imphal, India. Manuscript received: July 27, 2001; Initial review completed: September 18, 2001; Revision accepted: October 22, 2001. Porencephaly is a pseudocyst secondary to an infarct or other destructive cerebral lesion(1). It is a rare condition probably caused by vascular occlusion resulting from an insult during fetal development or an injury occurring later in life. It is often associated with various ophthalmic and neurologic signs including visual field defects, abnormal pupillary responses, optic nerve hypoplasia, decreased vision, nystagmus, strabismus, hemi-in-attention, seizures and mental deficiencies(2). There are two types of porencephaly: ( i ) Type I is generally due to an antepartum intraparenchymal hemorrhage; and (

38. Indian Pediatrics - Editorial
There is also evidence suggesting that unilateral Schizencephaly can be familialand probably accounts for previously reported familial porencephaly (13,14).
http://www.indianpediatrics.net/sept2001/sept-1049-1052.htm
Home Past Issue About IP About IAP ... Subscription Case Reports Indian Pediatrics 2001; 38: 949-951 Schizencephaly Type-I
A.K. Dubey, R.K. Gupta, P. Sharma*, R.K. Sharma
From the Departments of Pediatrics and Radiology, Base Hospital, Delhi Cantonment 110 010, India. Correspondence to: Dr. A.K. Dubey, Department of Pediatrics, Base Hospital, Delhi Cantonment 110 010, India.
E-mail: drdubey@yahoo.com Manuscript received: July 27, 2000;Initial review completed: September 21, 2000;Revision accepted: February 5, 2001. Amongst the cortical malformations, schizencephaly is more severe, yet restricted disorder(1,2). The lesion may be suspected by the appearance of focal ventricular dilatation on ultrasonogram and by visualization of gray matter lined cleft on CT Scan(3,4). However, the most sensitive modality for demonstration of schizencephaly is MRI(3,5). Of the two types of the schizencephaly described, Type I which consists of fused cleft without hydro-cephalus may not be detected by sonography, but is readily identified by CT/MRI(6,7). We report a case of Type I Schizencephaly for its rarity and to highlight sensitivity of MRI in demonstrating the lesion. Case Report An 11-year-old male child elder of the two siblings, was born at term to non-consan-guineous parents. Antenatal, intranatal and perinatal periods were uneventful. He pre-sented with global delay of motor milestones, frequent falls and weakness of the left half of the body since early infancy. There was no history of seizures. Scholastic performance of the child was within normal limits.

39. Directory :: Look.com
porencephaly (4) See Also. National Institute of Neurological Disordersand Stroke porencephaly information sheet compiled by NINDS.
http://www.look.com/searchroute/directorysearch.asp?p=527083

40. Volume 24 January - December 1901
A case of bilateral porencephaly. J . Wigglesworth. Pages 127 134. Part ofthe OUP Brain WWW service. General Information. Click here to register with OUP.
http://www3.oup.co.uk/jnls/supplements/braini/hdb/Volume_24/Issue_01/240127.sgm.
Volume 24: January - December 1901
Issue 1: 1901
Abstract
  • A case of bilateral porencephaly
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    Click here to register with OUP. This page is maintained by OUP admin Last updated 14 May 97 Part of the OUP Journals World Wide Web service Oxford University Press, 1997

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