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[Richards-Rundle syndrome].

Abstract
Among 43 female patients aged 17-46 years with almost severe oligophrenia there were four with primary hypogonadism, one of them a case of Richards Rundle syndrome, now aged 20 years with absence of secondary sex characters, hypoplastic genitals, deafness, ataxia, wasting of muscles and reduced jerks. In cases of hypogonadism and hypogenitalism should be searched for mental and neurologic disorders, also for genetic counseling of the siblings.
AuthorsP Fehlow, F Walther
JournalKlinische Padiatrie (Klin Padiatr) Vol. 203 Issue 3 Pg. 184-6 ( 1991) ISSN: 0300-8630 [Print] Germany
Vernacular TitleRichards-Rundle-Syndrom.
PMID1857055 (Publication Type: Case Reports, English Abstract, Journal Article)
Chemical References
  • Keto Acids
Topics
  • Adult
  • Ataxia (complications)
  • Deafness (complications)
  • Female
  • Genitalia, Female (abnormalities)
  • Humans
  • Hypogonadism (complications)
  • Intellectual Disability (complications)
  • Keto Acids (urine)
  • Muscular Atrophy (complications)

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