| Literature DB >> 10213038 |
M Masuno1, K Imaizumi, T Okada, M Adachi, G Nishimura, T Ishii, K Tachibana, Y Kuroki.
Abstract
Young-Simpson syndrome is a rare congenital disorder, characterized by congenital hypothyroidism, congenital heart defects, facial dysmorphism, cryptorchidism in males, hypotonia, mental retardation, and postnatal growth retardation. We describe the cases of a 5-year-old boy and a 7-year-old girl with a similar constellation of symptoms and compared them with previously reported patients.Entities:
Mesh:
Year: 1999 PMID: 10213038 DOI: 10.1002/(sici)1096-8628(19990507)84:1<8::aid-ajmg2>3.0.co;2-2
Source DB: PubMed Journal: Am J Med Genet ISSN: 0148-7299