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PMID: 3103548 Published · ppublish English Case Reports Journal Article

Noonan's syndrome and neurofibromatosis.

Archives of disease in childhood ·Vol. 62 ·No. 2 ·1987-02-00 ·Pages 196-8

Shuper A, Mukamel M, Mimouni M, Steinherz R

Abstract

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.

MeSH Terms
Child Humans Male Neurofibromatosis 1/complications Noonan Syndrome/complications Skin Neoplasms/complications
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Shuper A
Mukamel M
Mimouni M
Steinherz R
References (5)
5 references, click to expand
  1. Von Recklinghausen neurofibromatosis.
    N Engl J Med. 1981 Dec 31;305(27):1617-27 PMID: 6796886
  2. Noonan phenotype associated with neurofibromatosis.
    Am J Med Genet. 1985 Jul;21(3):457-62 PMID: 2411134
  3. Noonan syndrome: a review.
    Am J Med Genet. 1985 Jul;21(3):493-506 PMID: 3895929
  4. The neurofibromatosis-Noonan syndrome.
    Am J Med Genet. 1985 Jul;21(3):477-90 PMID: 3927726
  5. The neurofibromatosis-Noonan syndrome.
    Am J Med Genet. 1985 Jul;21(3):471-6 PMID: 3927725
Article Info
Journal
Archives of disease in childhood
Abbr.
Arch Dis Child
ISSN
1468-2044
Published
1987-02-00
Pages
196-8
Language
English
Region
England
NLM ID
0372434
PMCID
PMC1778243
Subset
IM
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