Literature DB >> 3911193

Prenatal diagnosis of Mohr syndrome by ultrasonography.

M Iaccarino, F Lonardo, M Giugliano, M D Della Bruna.   

Abstract

A case of prenatal diagnosis of Mohr syndrome is presented. The ultrasound examination was indicated by the previous birth of an affected brother. The need for genetic counselling is stressed, when polydactyly is observed accidentally at ultrasound examination during pregnancy.

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Mesh：

Year:  1985        PMID： 3911193     DOI： 10.1002/pd.1970050607

Source DB:  PubMed          Journal:  Prenat Diagn        ISSN： 0197-3851            Impact factor:   3.050


  4 in total

1.  A male with type I orofaciodigital syndrome.

Authors:  J Goodship; J Platt; R Smith; J Burn
Journal:  J Med Genet       Date:  1991-10       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.  Oral-facial-digital syndrome type 1 in males: Congenital heart defects are included in its phenotypic spectrum.

Authors:  Arjan Bouman; Mariëlle Alders; Roelof Jan Oostra; Elisabeth van Leeuwen; Nikki Thuijs; Anne-Marie van der Kevie-Kersemaekers; Merel van Maarle
Journal:  Am J Med Genet A       Date:  2017-04-03       Impact factor: 2.802
  4 in total

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