Literature DB >> 22802556

Cenani-Lenz syndrome-like limb anomaly with more severe involvement of left side.

Saleem Ahmed1, Jumana Yousef Al-Aama.   

Abstract

The authors describe a case of Cenani-Lenz syndrome, in a 3-month-old girl of non-consanguineous parents of Afghani origin. Digital anomalies consist of sandactyly of the fingers of both hands, disorganised phalanges more severe involvement of the left side without radioulnar synostosis. Although our patient lacks facial dysmorphic features reported previously. The cases of patients with CLS need to be carefully evaluated and described to determine if there is distinctive accompanying facial phenotype.

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Year:  2012        PMID: 22802556      PMCID: PMC3416989          DOI: 10.1136/bcr.01.2012.5634

Source DB:  PubMed          Journal:  BMJ Case Rep        ISSN: 1757-790X


  8 in total

1.  Cenani-Lenz syndrome with renal hypoplasia is not linked to FORMIN or GREMLIN.

Authors:  C Bacchelli; F R Goodman; P J Scambler; R M Winter
Journal:  Clin Genet       Date:  2001-03       Impact factor: 4.438

Review 2.  Cenani-Lenz syndrome: report of a new case and review of the literature.

Authors:  Marjan M Nezarati; D Ross McLeod
Journal:  Clin Dysmorphol       Date:  2002-07       Impact factor: 0.816

3.  Mild facial dysmorphism and quasidominant inheritance in Cenani-Lenz syndrome.

Authors:  Samia A Temtamy; Samira Ismail; Amany Nemat
Journal:  Clin Dysmorphol       Date:  2003-04       Impact factor: 0.816

4.  LRP4 mutations alter Wnt/beta-catenin signaling and cause limb and kidney malformations in Cenani-Lenz syndrome.

Authors:  Yun Li; Barbara Pawlik; Nursel Elcioglu; Mona Aglan; Hülya Kayserili; Gökhan Yigit; Ferda Percin; Frances Goodman; Gudrun Nürnberg; Asim Cenani; Jill Urquhart; Boi-Dinh Chung; Samira Ismail; Khalda Amr; Ayca D Aslanger; Christian Becker; Christian Netzer; Pete Scambler; Wafaa Eyaid; Hanan Hamamy; Jill Clayton-Smith; Raoul Hennekam; Peter Nürnberg; Joachim Herz; Samia A Temtamy; Bernd Wollnik
Journal:  Am J Hum Genet       Date:  2010-04-08       Impact factor: 11.025

5.  The genetics of hand malformations.

Authors:  S A Temtamy; V A McKusick
Journal:  Birth Defects Orig Artic Ser       Date:  1978

6.  Dermatoglyphics in patients with Cenani-Lenz type syndactyly: studies in a new case.

Authors:  N Elçioglu; M Atasu; A Cenani
Journal:  Am J Med Genet       Date:  1997-06-27

7.  [Total syndactylia and total radioulnar synostosis in 2 brothers. A contribution on the genetics of syndactylia].

Authors:  A Cenani; W Lenz
Journal:  Z Kinderheilkd       Date:  1967

8.  Genomic rearrangements of the GREM1-FMN1 locus cause oligosyndactyly, radio-ulnar synostosis, hearing loss, renal defects syndrome and Cenani--Lenz-like non-syndromic oligosyndactyly.

Authors:  Boyan Ivanov Dimitrov; Thierry Voet; Luc De Smet; Joris Robert Vermeesch; Koen Devriendt; Jean-Pierre Fryns; Philippe Debeer
Journal:  J Med Genet       Date:  2010-07-07       Impact factor: 6.318

  8 in total

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