Literature DB >> 7573149

Apparent Malpuech syndrome: report on three Brazilian patients with additional signs.

M L Guion-Almeida1.   

Abstract

We report on 3 unrelated Brazilian patients with shortness of stature, hypertelorism, eye anomalies, facial clefting, hearing loss, urogenital abnormalities, omphalocele, "caudal appendage," and mental retardation. Two patients were born to normal and non-consanguineous parents and one was born to consanguineous (first cousin) parents (F = 1/16). The similarity of our patients with those previously reported by Malpuech et al. [Am J Med Genet 16:475-480, 1983] led us to suggest that they have the same condition.

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Year:  1995        PMID: 7573149     DOI: 10.1002/ajmg.1320580104

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  2 in total

1.  MASP1 mutations in patients with facial, umbilical, coccygeal, and auditory findings of Carnevale, Malpuech, OSA, and Michels syndromes.

Authors:  Asli Sirmaci; Tom Walsh; Hatice Akay; Michail Spiliopoulos; Yıldırım Bayezit Sakalar; Aylin Hasanefendioğlu-Bayrak; Duygu Duman; Amjad Farooq; Mary-Claire King; Mustafa Tekin
Journal:  Am J Hum Genet       Date:  2010-10-28       Impact factor: 11.025

2.  Proposed caudal appendage classification system; spinal cord tethering associated with sacrococcygeal eversion.

Authors:  C Corbett Wilkinson; Arianne J Boylan
Journal:  Childs Nerv Syst       Date:  2016-08-06       Impact factor: 1.475

  2 in total

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