Literature DB >> 8588856

Coffin-Lowry syndrome: clinical aspects at different ages and symptoms in female carriers.

A S Plomp1, C E De Die-Smulders, P Meinecke, J M Ypma-Verhulst, D A Lissone, J P Fryns.   

Abstract

We present three patients with the Coffin-Lowry syndrome, two males aged 21 years and 14 months respectively, and an unrelated girl aged 11 years. In the male patients the features at different ages are reviewed. Besides, we describe the pertinent features of their affected female relatives. The contribution of the family history to making the diagnosis is stressed. The isolated female proband is much more severely affected than the female relatives of the male probands, demonstrating that the clinical picture in female carriers of Coffin-Lowry syndrome can vary considerably. The differential diagnosis of Coffin-Lowry syndrome will be discussed shortly.

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Year:  1995        PMID: 8588856

Source DB:  PubMed          Journal:  Genet Couns        ISSN: 1015-8146


  4 in total

1.  Unusual splice-site mutations in the RSK2 gene and suggestion of genetic heterogeneity in Coffin-Lowry syndrome.

Authors:  Maria Zeniou; Solange Pannetier; Jean-Pierre Fryns; André Hanauer
Journal:  Am J Hum Genet       Date:  2002-04-25       Impact factor: 11.025

2.  Short Bones, Renal Stones, and Diagnostic Moans: Hypercalcemia in a Girl Found to Have Coffin-Lowry Syndrome.

Authors:  Christina G Tise; Dena R Matalon; Melanie A Manning; Heather M Byers; Monica Grover
Journal:  J Investig Med High Impact Case Rep       Date:  2022 Jan-Dec

3.  Delineation of the mechanisms of aberrant splicing caused by two unusual intronic mutations in the RSK2 gene involved in Coffin-Lowry syndrome.

Authors:  Maria Zeniou; Renata Gattoni; André Hanauer; James Stévenin
Journal:  Nucleic Acids Res       Date:  2004-02-18       Impact factor: 16.971

Review 4.  Coffin-Lowry syndrome: clinical and molecular features.

Authors:  A Hanauer; I D Young
Journal:  J Med Genet       Date:  2002-10       Impact factor: 6.318

  4 in total

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