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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

81. Lab Study 6
A80377 Congenital porencephaly, bilateral and HI-88 Congenital porencephaly,bilateral (pp. 821-824) porencephaly is a defect that occurs in utero.
http://www.musc.edu/pathology/teaching/LabStudy/LS6.htm
LAB STUDY 6 CAL: Review previous CAL's Microscopic slides: No new slides Neuropathology Museum Specimen Tour: Anencephaly (p. 821-824)
is the most common congenital brain malformation.
Note "froglike" facies and the cerebrovascularis on the back of the head. The occipital bone is usually absent.
How long does a newborn usually survive? A77-503 Holoprosencephaly (pp. 821-824)
What Greek mythology figure is "associated" with this condition?
Is a chromosomal abnormality always involved? A80-377 Congenital porencephaly, bilateral and HI-88 Congenital porencephaly, bilateral (pp. 821-824)
Porencephaly is a defect that occurs in utero. The cause may be ischemia or hemorrhage. It is a large cavitary/cystic defect of the cerebral hemisphere(s) resulting from the destruction of both the cortex and white matter. These lesions are frequently bilateral.
What percentage of newborns have major congenital malformations? Of these, how many are in the CNS? A80-34 Atrophy and microcephaly
What is atrophy? Note the narrowed gyri and widened sulci.

82. Porencephaly
Navigation. Selected medical images OMIM porencephaly Porencephaliccyst; porencephaly; porencephaly of the Brain; Unilateral porencephaly;
http://www.gfmer.ch/Genetic_diseases/Porencephaly/porencephaly.htm
Geneva Foundation for Medical Education and Research Home About Search Medical education ...
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Porencephaly Sources
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Edited by Aldo Campana, March 13, 2003

83. Cephalic Disorders:acephaly,anencephaly,brachycephaly,cebocephaly,colprocephaly,
macrencephaly,macrocephaly,megalencephaly,microcephaly,micrencephaly,octocephaly,oxycephaly,plagiocephaly,porencephaly,schapocephaly,schizencephaly
http://www.icomm.ca/geneinfo/cephaly.htm
The GAPS INDEX
to Information on the Internet about Genetic Disorders and Birth Defects

Genetic Information and Patient Services, Inc. (GAPS)
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DISORDERS GLOSSARY Cephalic Disorders
(as defined by the National Institute of Neurological Disorders and Stroke, NIH What Are Cephalic Disorders? Cephalic disorders are congenital conditions that stem from damage to, or abnormal development of, the budding nervous system. Cephalic is a term that means "head" or "head end of the body." Congenital means the disorder is present at, and usually before, birth. Although there are many congenital developmental disorders, this fact sheet briefly describes only cephalic conditions. Cephalic disorders are not necessarily caused by a single factor, but may be influenced by hereditary or genetic conditions, or by environmental exposures during pregnancy such as medication taken by the mother, maternal infection, or exposure to radiation. Some cephalic disorders occur when the cranial sutures (the fibrous joints that connect the bones of the skull) join prematurely. Most cephalic disorders are caused by a disturbance that occurs very early in the development of the fetal nervous system. The human nervous system develops from a small, specialized plate of cells on the surface of the embryo. Early in development, this plate of cells forms the

84. IComm: File Not Found!
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85. Untitled
and culture. P0601. Familial Orofaciodigital syndrome type I revealedby ultrasound diagnosis of porencephaly. C. ThauvinRobinet
http://mail.medacad.org/www.ichg2001.org/abstracts/prenatal.htm
Posters P0594-P0704 - Prenatal and Perinatal Genetics 594. Fetal cells in maternal blood as a screening test for fetal aneuploidies A. Mavrou , A. Kolialexi , A. Antsaklis , A. Koratzis , C. Metaxotou Medical Genetics Athens University School of Medicine; Athens, Greece; Medical Genetics, Athens University, School of Medicine; Athens, Greece; Medical Genetics, Athens University school of Medicine; Athens, Greece ariamav@hol.gr Anti hemoglobin chain antibody has been used to detect fetal nucleated red blood cells (NRBCs) entering maternal circulation during pregnancy. In a previous study we demonstrated, however, that women carriers of -thalassemia produce themselves during pregnancy an increased number of + NRBC making it difficult to distinguish between fetal and maternal NRBCs. Use of Ab against embryonic hemoglobin may increase specificity for fetal NRBCs. In the present study NRBCs were isolated by MACS from 20ml peripheral blood of 50 pregnant women carriers of thalassemia trait, 27 in the first and 23 in the second trimester of pregnancy. NRBCs were next identified immunocytochemically using anti or anti monoclonal antibodies (MoAb). FISH was performed in 22 cases known to carry male fetuses with X/Y chromosome specific probes. The mean number of NRBCs isolated with anti

86. Cephalic Disorders - Neurologychannel
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CEPHALIC DISORDERS
Overview

Anencephaly

Colpocephaly

Holoprosencephaly
...
Other Types
CONDITIONS
ADHD

ALS

Alzheimer's Disease
Autism ... Carpal Tunnel Syndrome Cephalic Disorders Cerebral Palsy Charcot-Marie-Tooth Disease Dementia Encephalitis Epilepsy Essential Tremor ... Guillain-Barre Syndrome Headache Huntington's Disease Hydrocephalus Lou Gehrig's Disease ... Traumatic Brain Injury Vertigo TREATMENT OPTIONS
Botulinum Toxin Therapy Epidural Injection Trigger Point Injection Vagus Nerve Stimulation RESOURCES Clinical Trials Links Videos ABOUT US Healthcommunities.com Pressroom Testimonial Overview The term cephalic disorders refers to defects resulting from abnormal development of, or damage to, the brain and spinal cord. Cephalic disorders are present at or before birth. In most cases, the problem occurs early in the development of the fetal nervous system. In other cases, the problem occurs when the fibrous joints connecting the bones of the skull join prematurely. Cephalic disorders may be caused by genetic conditions or by exposure of the mother and developing fetus to infections, toxic substances, medications, or radiation. The severity of these disorders varies greatly. Some cause mild disabilities; others are profound, resulting in total lifelong disability, vastly reduced functional capacity, and sometimes death.

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