Literature DB >> 2325097

Orofaciodigital syndrome type IV (Mohr-Majewski syndrome) with severe expression expanding the known spectrum of anomalies.

P Meinecke1, H Hayek.   

Abstract

We present a male infant with hypertelorism, median pseudo-cleft of the upper lip and cleft palate, lobulated tongue, hypoplastic larynx and epiglottis, mesomelic shortening of limbs with particularly short and broad tibiae, polydactyly of the upper limbs, severely hypoplastic external genitalia with anorchidism, anal atresia, severe congenital heart defect, and renal agenesis. These features show considerable overlap with severe Majewski type short rib-polydactyly syndrome and so expand the known spectrum of anomalies in orofaciodigital syndrome type IV.

Entities:  

Mesh:

Year:  1990        PMID: 2325097      PMCID: PMC1017006          DOI: 10.1136/jmg.27.3.200

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  5 in total

1.  Orofaciodigital syndrome with mesomelic limb shortening.

Authors:  J Burn; C Dezateux; C M Hall; M Baraitser
Journal:  J Med Genet       Date:  1984-06       Impact factor: 6.318

2.  A female infant with features of Mohr and Majewski syndromes: variable expression, a genetic compound, or a distinct entity?

Authors:  M Baraitser; J Burn; J Fixsen
Journal:  J Med Genet       Date:  1983-02       Impact factor: 6.318

3.  Orofaciodigital syndrome type IV: report of a patient.

Authors:  N C Nevin; P S Thomas
Journal:  Am J Med Genet       Date:  1989-02

4.  Oro-facial-digital syndrome II. Transitional type between the Mohr and the Majewski syndromes: report of two new cases.

Authors:  M C Silengo; G L Bell; M Biagioli; P Franceschini
Journal:  Clin Genet       Date:  1987-05       Impact factor: 4.438

5.  X-linked recessive inheritance of an orofaciodigital syndrome with partial expression in females and survival of affected males.

Authors:  M Edwards; D Mulcahy; G Turner
Journal:  Clin Genet       Date:  1988-11       Impact factor: 4.438

  5 in total
  4 in total

1.  Hydrometrocolpos and polydactyly: a common neonatal presentation of Bardet-Biedl and McKusick-Kaufman syndromes.

Authors:  A David; P Bitoun; D Lacombe; J C Lambert; A Nivelon; J Vigneron; A Verloes
Journal:  J Med Genet       Date:  1999-08       Impact factor: 6.318

2.  Orocardiodigital syndrome: an oral-facial-digital type II variant associated with atrioventricular canal.

Authors:  M C Digilio; B Marino; A Giannotti; B Dallapiccola
Journal:  J Med Genet       Date:  1996-05       Impact factor: 6.318

3.  The many faces of oral-facial-digital syndrome.

Authors:  E Sukarova-Angelovska; N Angelkova; S Palcevska-Kocevska; M Kocova
Journal:  Balkan J Med Genet       Date:  2012-06       Impact factor: 0.519

4.  Craniodentofacial Manifestations in a Rare Syndrome: Orofaciodigital Type IV (Mohr-Majewski Syndrome).

Authors:  Meltem Ozdemir-Karatas; Didem Ozdemir-Ozenen; P Suzanne Hart; Thomas C Hart
Journal:  Case Rep Dent       Date:  2014-12-21
  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.