| Literature DB >> 19772821 |
Beata Wikiera1, Ewa Głab, Ryszard Slezak, Elzbieta Wójcik, Anna Noczyńska.
Abstract
49,XXXXY syndrome is a very rare sex chromosomes polysomy, which is always connected with dysmorphic appearance, hypergonadothrophic hypogonadism and mental retardation. In this report we describe the clinical, biochemical, hormonal, radiological and developmental status of the patient with 49,XXXXY syndrome, referred to our department at the age of 12 months because of underdeveloped external genitalia. Subclinical hypothyroidism and severe scoliosis could further disturb his development.Entities:
Mesh:
Year: 2009 PMID: 19772821
Source DB: PubMed Journal: Pediatr Endocrinol Diabetes Metab ISSN: 2083-8441