Noonan's syndrome and neurofibromatosis

A child with Noonan syndrome and multiple cafe au lait spots, compatible in size and number with von Recklinghausen's neurofibromatosis, is presented. These features may represent a distinct genetic entity rather than the coincidence of two diseases.

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Bibliographic Details
Published inArchives of disease in childhood Vol. 62; no. 2; pp. 196 - 198
Main Authors Shuper, A, Mukamel, M, Mimouni, M, Steinherz, R
Format Journal Article
LanguageEnglish
Published London BMJ Publishing Group Ltd and Royal College of Paediatrics and Child Health 01.02.1987
BMJ
BMJ Publishing Group LTD
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Summary:A child with Noonan syndrome and multiple cafe au lait spots, compatible in size and number with von Recklinghausen's neurofibromatosis, is presented. These features may represent a distinct genetic entity rather than the coincidence of two diseases.
Bibliography:istex:3D017E94C069613EAF257EFEDE4E5C648EC72F6A
ark:/67375/NVC-NCK15P4H-0
PMID:3103548
local:archdischild;62/2/196
href:archdischild-62-196.pdf
ObjectType-Case Study-2
SourceType-Scholarly Journals-1
ObjectType-Feature-4
content type line 23
ObjectType-Report-1
ObjectType-Article-3
ISSN:0003-9888
1468-2044
DOI:10.1136/adc.62.2.196