Literature DB >> 10213038

Young-Simpson syndrome: further delineation of a distinct syndrome with congenital hypothyroidism, congenital heart defects, facial dysmorphism, and mental retardation.

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.

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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


  1 in total

1.  Chronic Otitis Media Associated with Cholesteatoma in a Case of the Say-Barber-Biesecker-Young-Simpson Variant of Ohdo Syndrome.

Authors:  Bruno Galletti; Francesco Gazia; Francesco Freni; Rita Angela Nicita; Rocco Bruno; Francesco Galletti
Journal:  Am J Case Rep       Date:  2019-02-10
  1 in total

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