These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
Pubmed for Handhelds
PUBMED FOR HANDHELDS
Search MEDLINE/PubMed
Title: Smith-Fineman-Myers syndrome in two brothers. Author: Adès LC, Kerr B, Turner G, Wise G. Journal: Am J Med Genet; 1991 Sep 15; 40(4):467-70. PubMed ID: 1684092. Abstract: We report on 2 brothers with a distinctive facial appearance, severe mental retardation, short stature, cryptorchidism, asplenia in one, dramatic failure to thrive, early hypotonia, and later hypertonia all suggestive of the Smith-Fineman-Myers syndrome. All 5 of the reported cases have been males, suggesting X-linked inheritance.[Abstract] [Full Text] [Related] [New Search]