Literature DB >> 6829615

Familial X-linked mental retardation syndrome associated with minor congenital anomalies, macro-orchidism, and fragile X-chromosome.

S M Pueschel, R M Hays, T Mendoza.   

Abstract

Three young males of Azorian origin who exhibited significant mental retardation, minor congenital anomalies, behavior disorders, and macro-orchidism were described. The chromosomal analysis revealed a fragile X chromosome in all three patients.

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Year:  1983        PMID: 6829615

Source DB:  PubMed          Journal:  Am J Ment Defic        ISSN: 0002-9351


  4 in total

1.  Brief report: screening children with autism for fragile-X syndrome and phenylketonuria.

Authors:  S M Pueschel; R Herman; G Groden
Journal:  J Autism Dev Disord       Date:  1985-09

2.  Neurological findings in patients with the fragile-X syndrome.

Authors:  P F Finelli; S M Pueschel; T Padre-Mendoza; M M O'Brien
Journal:  J Neurol Neurosurg Psychiatry       Date:  1985-02       Impact factor: 10.154

3.  Intelligence and cognitive profile in the fra(X) syndrome: a longitudinal study in 18 fra(X) boys.

Authors:  L M Curfs; G Schreppers-Tijdink; A Wiegers; M Borghgraef; J P Fryns
Journal:  J Med Genet       Date:  1989-07       Impact factor: 6.318

4.  Thyroid function in fragile-X syndrome males.

Authors:  J D Bregman; J F Leckman; S I Ort
Journal:  Yale J Biol Med       Date:  1990 Jul-Aug
  4 in total

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