Literature DB >> 12868467

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

Samia A Temtamy1, Samira Ismail, Amany Nemat.   

Abstract

Cenani-Lenz syndrome (CLS; MIM 212780) is a rare autosomal recessive syndactyly/synostosis syndrome. No facial dysmorphism was previously noted. We studied two families; in the first an affected female had a previously affected brother and her father was said to have been similarly affected. Extensive inbreeding in this family suggests quasidominant inheritance. In the second family there was a history of a similarly affected sib who, in addition, had genital anomalies and cleft palate. The parents were first cousins. Both probands had similar mild facial dysmorphism; a high broad, prominent forehead, hypertelorism, a depressed nasal bridge, downslanting palpebral fissures, a short nose, a short prominent philtrum and malar hypoplasia. The present report suggests mild facial dysmorphism and quasidominant inheritance in one family with Cenani-Lenz syndrome.

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Year:  2003        PMID: 12868467     DOI: 10.1097/00019605-200304000-00001

Source DB:  PubMed          Journal:  Clin Dysmorphol        ISSN: 0962-8827            Impact factor:   0.816


  5 in total

1.  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

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

Authors:  Saleem Ahmed; Jumana Yousef Al-Aama
Journal:  BMJ Case Rep       Date:  2012-07-13

3.  Mutations in the fourth β-propeller domain of LRP4 are associated with isolated syndactyly with fusion of the third and fourth fingers.

Authors:  Rivka Sukenik Halevy; Huan-Chieh Chien; Bo Heinz; Michael J Bamshad; Deborah A Nickerson; Martin Kircher; Nadav Ahituv
Journal:  Hum Mutat       Date:  2018-03-22       Impact factor: 4.878

Review 4.  Syndactyly: phenotypes, genetics and current classification.

Authors:  Sajid Malik
Journal:  Eur J Hum Genet       Date:  2012-02-15       Impact factor: 4.246

5.  Cenani-Lenz syndactyly syndrome - a case report of a family with isolated syndactyly.

Authors:  Dineshani Hettiaracchchi; Carine Bonnard; S M A Jayawardana; Alvin Yu Jin Ng; Sumanty Tohari; Byrappa Venkatesh; Bruno Reversade; Roshni Singaraja; V H W Dissanayake
Journal:  BMC Med Genet       Date:  2018-07-24       Impact factor: 2.103

  5 in total

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