Literature DB >> 19772821

Sex chromosome pentasomy 49,XXXXY connected with hypothyroidism. Case report.

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.

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Year:  2009        PMID: 19772821

Source DB:  PubMed          Journal:  Pediatr Endocrinol Diabetes Metab        ISSN: 2083-8441


  2 in total

1.  Case report of 49,XXXXY syndrome with cleft palate, diabetes, hypothyroidism, and cataracts.

Authors:  Limin Wei; Yi Liu; Sufen Sun; Yong Tang; Shuchun Chen; Guangyao Song
Journal:  Medicine (Baltimore)       Date:  2019-09       Impact factor: 1.817

2.  Testosterone replacement in 49,XXXXY syndrome: andrological, metabolic and neurological aspects.

Authors:  Rossella Mazzilli; Michele Delfino; Jlenia Elia; Francesco Benedetti; Laura Alesi; Luciana Chessa; Fernando Mazzilli
Journal:  Endocrinol Diabetes Metab Case Rep       Date:  2015-12-23
  2 in total

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