| The macrocephaly-cutis marmorata telangiectatica congenita syndrome. Long-term follow-up data in 4 children and adolescents. | |
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MedLine Citation:
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PMID: 9894160 Owner: NLM Status: MEDLINE |
Abstract/OtherAbstract:
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We present the clinical history and findings in 4 children and adolescents with the association of macrocephaly and cutis marmorata telangiectatica congenita (Macrocephaly-CMTC syndrome). This syndrome has recently been delineated within the general group of patients with manifestations of cutis marmorata telangiectatica-Klippel-Trenaunay-Weber syndrome as a clinically recognisable entity. |
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Authors:
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A Vogels; K Devriendt; E Legius; P Decock; J Marien; G Hendrickx; J P Fryns |
Publication Detail:
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Type: Journal Article |
Journal Detail:
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Title: Genetic counseling (Geneva, Switzerland) Volume: 9 ISSN: 1015-8146 ISO Abbreviation: Genet. Couns. Publication Date: 1998 |
Date Detail:
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Created Date: 1999-04-14 Completed Date: 1999-04-14 Revised Date: 2006-07-06 |
Medline Journal Info:
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Nlm Unique ID: 9015261 Medline TA: Genet Couns Country: SWITZERLAND |
Other Details:
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Languages: eng Pagination: 245-53 Citation Subset: IM |
Affiliation:
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Center for Human Genetics, Leuven, Belgium. |
Export Citation:
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| MeSH Terms | |
Descriptor/Qualifier:
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Adolescent Cephalometry Child Child, Preschool Craniofacial Abnormalities / diagnosis, genetics* Follow-Up Studies Humans Infant Infant, Newborn Male Mental Retardation / diagnosis, genetics Muscle Hypotonia / diagnosis, genetics Skin Diseases, Genetic / diagnosis, genetics* Syndrome Telangiectasia, Hereditary Hemorrhagic / diagnosis, genetics* |
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
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