Literature DB >> 671157

Confirmation of the Cohen syndrome.

J C Carey, B D Hall.   

Abstract

In 1973 Cohen et al reported a new syndrome in two siblings and an unrelated individual, consisting of obesity, mental retardation, hypotonia, limb abnormalities, and a characteristic craniofacial appearance. Since then no similar cases have appeared in the literature. This report firmly establishes the Cohen syndrome as a distinct clinical entity by presenting four additional patients, including a sibling pair of normal parents, suggesting autosomal recessive inheritance. One of our four patients has normal intelligence, indicating that mental deficiency is a variable feature of the syndrome.

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Year:  1978        PMID: 671157     DOI: 10.1016/s0022-3476(78)80504-6

Source DB:  PubMed          Journal:  J Pediatr        ISSN: 0022-3476            Impact factor:   4.406


  11 in total

1.  Cohen syndrome is caused by mutations in a novel gene, COH1, encoding a transmembrane protein with a presumed role in vesicle-mediated sorting and intracellular protein transport.

Authors:  Juha Kolehmainen; Graeme C M Black; Anne Saarinen; Kate Chandler; Jill Clayton-Smith; Ann-Liz Träskelin; Rahat Perveen; Satu Kivitie-Kallio; Reijo Norio; Mette Warburg; Jean-Pierre Fryns; Albert de la Chapelle; Anna-Elina Lehesjoki
Journal:  Am J Hum Genet       Date:  2003-05-02       Impact factor: 11.025

2.  Diagnostic criteria, clinical characteristics, and natural history of Cohen syndrome.

Authors:  K E Chandler; A Kidd; L Al-Gazali; J Kolehmainen; A-E Lehesjoki; G C M Black; J Clayton-Smith
Journal:  J Med Genet       Date:  2003-04       Impact factor: 6.318

3.  The clinical features of the Cohen syndrome: further case reports.

Authors:  C North; M A Patton; M Baraitser; R M Winter
Journal:  J Med Genet       Date:  1985-04       Impact factor: 6.318

4.  The Cohen syndrome: clinical and endocrinological studies of two new cases.

Authors:  P Balestrazzi; L Corrini; G Villani; M P Bolla; F Casa; S Bernasconi
Journal:  J Med Genet       Date:  1980-12       Impact factor: 6.318

5.  High frequency of COH1 intragenic deletions and duplications detected by MLPA in patients with Cohen syndrome.

Authors:  Veronica Parri; Eleni Katzaki; Vera Uliana; Francesca Scionti; Rossella Tita; Rosangela Artuso; Ilaria Longo; Renske Boschloo; Raymon Vijzelaar; Angelo Selicorni; Francesco Brancati; Bruno Dallapiccola; Leopoldo Zelante; Christian P Hamel; Pierre Sarda; Seema R Lalani; Rita Grasso; Sabrina Buoni; Joussef Hayek; Laurent Servais; Bert B A de Vries; Nelly Georgoudi; Sheena Nakou; Michael B Petersen; Francesca Mari; Alessandra Renieri; Francesca Ariani
Journal:  Eur J Hum Genet       Date:  2010-05-12       Impact factor: 4.246

6.  Clinical and molecular characterization of Italian patients affected by Cohen syndrome.

Authors:  Eleni Katzaki; Chiara Pescucci; Vera Uliana; Filomena Tiziana Papa; Francesca Ariani; Ilaria Meloni; Manuela Priolo; Angelo Selicorni; Donatella Milani; Rita Fischetto; Maria Elena Celle; Rita Grasso; Bruno Dallapiccola; Francesco Brancati; Marta Bordignon; Romano Tenconi; Antonio Federico; Francesca Mari; Alessandra Renieri; Ilaria Longo
Journal:  J Hum Genet       Date:  2007-11-08       Impact factor: 3.172

7.  The ophthalmic findings in Cohen syndrome.

Authors:  K E Chandler; S Biswas; I C Lloyd; N Parry; J Clayton-Smith; G C M Black
Journal:  Br J Ophthalmol       Date:  2002-12       Impact factor: 4.638

8.  Mental retardation, hypotonia, obesity, ocular, facial, dental, and limb abnormalities (Cohen syndrome). Report of three patients.

Authors:  T Goecke; F Majewski; K D Kauther; U Sterzel
Journal:  Eur J Pediatr       Date:  1982-07       Impact factor: 3.183

9.  Growth hormone deficiency in a girl with the Cohen syndrome.

Authors:  G Massa; L Dooms; M Vanderschueren-Lodeweyckx
Journal:  J Med Genet       Date:  1991-01       Impact factor: 6.318

Review 10.  Cohen Syndrome: Review of the Literature.

Authors:  Jonathan M Rodrigues; Hermina D Fernandes; Carrie Caruthers; Stephen R Braddock; Alan P Knutsen
Journal:  Cureus       Date:  2018-09-18
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