Literature DB >> 6541982

Early clinical signs in Coffin-Lowry syndrome.

J S Vles, M Haspeslagh, M M Raes, J P Fryns, P Casaer, E Eggermont.   

Abstract

Two unrelated patients with Coffin-Lowry syndrome are described. The main characteristics of a typical face, thick hands with tapering fingers and a transverse hypothenar crease, general hypotonia with extensible joints made diagnosis possible before the age of 6 months. A persistent large anterior fontanel beyond the age of two years may be another associated finding. Retarded bone age, coarsity of the face and skeletal malformations considered characteristic in adult patients were not present. Early recognition of Coffin-Lowry syndrome is important for genetic counseling and prevention of severe skeletal malformations.

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Year:  1984        PMID: 6541982     DOI: 10.1111/j.1399-0004.1984.tb01087.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  2 in total

1.  Callosal dysgenesis in a patient with Coffin-Lowry syndrome.

Authors:  A Ozden; E Dirik; A Emel; N Sevinc
Journal:  Indian J Pediatr       Date:  1994 Jan-Feb       Impact factor: 1.967

2.  A syndrome of hypotonia, psychomotor retardation, seizures, delayed and dysharmonic skeletal maturation, and congenital fibre type disproportion.

Authors:  Q H Qazi; D Markouizos; C Rao; T Sheikh; E Beller; R Kula
Journal:  J Med Genet       Date:  1994-05       Impact factor: 6.318

  2 in total

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