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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
6
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pubmed:dateCreated |
2006-6-2
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pubmed:abstractText |
Mutations of the filamin A locus (FLNA) on Xq28 have been established in girls with periventricular nodular heterotopia and in patients with otopalatodigital and overlapping phenotypes, the pathogenesis of these phenotypes being thought to be quite distinct. To date only six male cases of periventricular nodular heterotopia (PVNH) have been reported and these almost invariably associated with severe neurological signs.
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pubmed:commentsCorrections |
http://linkedlifedata.com/resource/pubmed/commentcorrection/16299064-10327244,
http://linkedlifedata.com/resource/pubmed/commentcorrection/16299064-11078572,
http://linkedlifedata.com/resource/pubmed/commentcorrection/16299064-11311000,
http://linkedlifedata.com/resource/pubmed/commentcorrection/16299064-11532987,
http://linkedlifedata.com/resource/pubmed/commentcorrection/16299064-11694544,
http://linkedlifedata.com/resource/pubmed/commentcorrection/16299064-11914408,
http://linkedlifedata.com/resource/pubmed/commentcorrection/16299064-12393796,
http://linkedlifedata.com/resource/pubmed/commentcorrection/16299064-12612583,
http://linkedlifedata.com/resource/pubmed/commentcorrection/16299064-1427786,
http://linkedlifedata.com/resource/pubmed/commentcorrection/16299064-14988809,
http://linkedlifedata.com/resource/pubmed/commentcorrection/16299064-15194946,
http://linkedlifedata.com/resource/pubmed/commentcorrection/16299064-15249610,
http://linkedlifedata.com/resource/pubmed/commentcorrection/16299064-15459826,
http://linkedlifedata.com/resource/pubmed/commentcorrection/16299064-8290091,
http://linkedlifedata.com/resource/pubmed/commentcorrection/16299064-8562093,
http://linkedlifedata.com/resource/pubmed/commentcorrection/16299064-8644737,
http://linkedlifedata.com/resource/pubmed/commentcorrection/16299064-8787433,
http://linkedlifedata.com/resource/pubmed/commentcorrection/16299064-9883725
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Jun
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pubmed:issn |
1468-6244
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pubmed:author |
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pubmed:issnType |
Electronic
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pubmed:volume |
43
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
541-4
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pubmed:dateRevised |
2009-11-18
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pubmed:meshHeading |
pubmed-meshheading:16299064-Abnormalities, Multiple,
pubmed-meshheading:16299064-Adult,
pubmed-meshheading:16299064-Cerebral Ventricles,
pubmed-meshheading:16299064-Child, Preschool,
pubmed-meshheading:16299064-Choristoma,
pubmed-meshheading:16299064-Constipation,
pubmed-meshheading:16299064-Contractile Proteins,
pubmed-meshheading:16299064-Craniofacial Abnormalities,
pubmed-meshheading:16299064-DNA Mutational Analysis,
pubmed-meshheading:16299064-Diagnosis, Differential,
pubmed-meshheading:16299064-Female,
pubmed-meshheading:16299064-Humans,
pubmed-meshheading:16299064-Infant,
pubmed-meshheading:16299064-Infant, Newborn,
pubmed-meshheading:16299064-Magnetic Resonance Imaging,
pubmed-meshheading:16299064-Male,
pubmed-meshheading:16299064-Microfilament Proteins,
pubmed-meshheading:16299064-RNA Splicing,
pubmed-meshheading:16299064-Syndrome
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pubmed:year |
2006
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pubmed:articleTitle |
A filamin A splice mutation resulting in a syndrome of facial dysmorphism, periventricular nodular heterotopia, and severe constipation reminiscent of cerebro-fronto-facial syndrome.
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pubmed:publicationType |
Letter,
Case Reports,
Research Support, Non-U.S. Gov't
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