| Neurocutaneous disorders in children. | |
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MedLine Citation:
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PMID: 8374670 Owner: NLM Status: MEDLINE |
Abstract/OtherAbstract:
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Neurocutaneous syndromes are disorders with cutaneous and neurologic anomalies. Some of these disorders are hereditary. This review summarizes the advances in this field and the recent results obtained in clinical and scientific research on the following syndromes: neurofibromatosis type 1, tuberous sclerosis, Gorlin-Goltz syndrome (nevoid basal cell carcinoma syndrome), Sjögren-Larsson syndrome, trichothiodystrophy, incontinentia pigmenti, CHILD (congenital hemidysplasia with ichthyosiform nevus and limb defects) syndrome, Menkes' syndrome, encephalocraniocutaneous lipomatosis, Proteus syndrome, Sturge-Weber syndrome, and so-called hypomelanosis of lto. |
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Authors:
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W Küster; R Happle |
Publication Detail:
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Type: Journal Article; Review |
Journal Detail:
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Title: Current opinion in pediatrics Volume: 5 ISSN: 1040-8703 ISO Abbreviation: Curr. Opin. Pediatr. Publication Date: 1993 Aug |
Date Detail:
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Created Date: 1993-10-15 Completed Date: 1993-10-15 Revised Date: 2005-11-16 |
Medline Journal Info:
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Nlm Unique ID: 9000850 Medline TA: Curr Opin Pediatr Country: UNITED STATES |
Other Details:
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Languages: eng Pagination: 436-40 Citation Subset: IM |
Affiliation:
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University of Marburg, Germany. |
Export Citation:
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| MeSH Terms | |
Descriptor/Qualifier:
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Basal Cell Nevus Syndrome Child Humans Incontinentia Pigmenti Menkes Kinky Hair Syndrome Nervous System Diseases* / etiology Neurofibromatosis 1 Proteus Syndrome Sjogren-Larsson Syndrome Skin Diseases* / etiology Sturge-Weber Syndrome Tuberous Sclerosis |
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
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