Literature DB >> 20145678

Mammary-digital-nail (MDN) syndrome: a novel phenotype maps to human chromosome 22q12.3-13.1.

Mira Genzer-Nir1, Morad Khayat, Leonid Kogan, Hector I Cohen, Miriam Hershkowitz, Dan Geiger, Tzipora C Falik-Zaccai.   

Abstract

Mammary-digital-nail syndrome is a novel phenotypic association consisting of anonychia onychodystrophy with hypoplasia or absence of distal phalanges in males and females, accompanied by juvenile hypertrophy of the breast in affected females. This newly described genetic trait presents an autosomal dominant inheritance pattern, with either reduced penetrance or germ-line mosaicism. Analysis of the pedigree, linkage studies followed by a genome-wide screen and by haplotype analysis defined the locus for the phenotype within a 12 cM (4.3 Mb) interval on chromosome 22q12.3-13.1. This chromosomal region has not been implicated before in genetic disorders of the mammary tissue or limbs. These data suggest a possibly novel signaling pathway affecting the organogenesis of limbs and mammary glands in humans.

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Year:  2010        PMID: 20145678      PMCID: PMC2987341          DOI: 10.1038/ejhg.2009.236

Source DB:  PubMed          Journal:  Eur J Hum Genet        ISSN: 1018-4813            Impact factor:   4.246


  24 in total

Review 1.  New genetic principles.

Authors:  Yuval Yaron; Avi Orr-Urtreger
Journal:  Clin Obstet Gynecol       Date:  2002-09       Impact factor: 2.190

2.  Optimizing exact genetic linkage computations.

Authors:  Ma'ayan Fishelson; Dan Geiger
Journal:  J Comput Biol       Date:  2004       Impact factor: 1.479

3.  Limb mammary syndrome: a new genetic disorder with mammary hypoplasia, ectrodactyly, and other Hand/Foot anomalies maps to human chromosome 3q27.

Authors:  H van Bokhoven; M Jung; A P Smits; S van Beersum; F Rüschendorf; M van Steensel; M Veenstra; J H Tuerlings; E C Mariman; H G Brunner; T F Wienker; A Reis; H H Ropers; B C Hamel
Journal:  Am J Hum Genet       Date:  1999-02       Impact factor: 11.025

Review 4.  Germ line mosaicism.

Authors:  J Zlotogora
Journal:  Hum Genet       Date:  1998-04       Impact factor: 4.132

Review 5.  Relationship between genotype and phenotype in monogenic diseases: relevance to polygenic diseases.

Authors:  K M Summers
Journal:  Hum Mutat       Date:  1996       Impact factor: 4.878

Review 6.  Juvenile breast hypertrophy: report of a familial pattern and review of the literature.

Authors:  D Kupfer; D Dingman; R Broadbent
Journal:  Plast Reconstr Surg       Date:  1992-08       Impact factor: 4.730

7.  Anonychia and absence/hypoplasia of distal phalanges (Cooks syndrome): report of a second family.

Authors:  N C Nevin; P S Thomas; D J Eedy; C Shepherd
Journal:  J Med Genet       Date:  1995-08       Impact factor: 6.318

8.  A new nail dysplasia syndrome with onychonychia and absence and/or hypoplasia of distal phalanges.

Authors:  R G Cooks; M Hertz; M B Katznelson; R M Goodman
Journal:  Clin Genet       Date:  1985-01       Impact factor: 4.438

9.  Familial juvenile hypertrophy of the breast.

Authors:  Jacky Govrin-Yehudain; Leonid Kogan; Hector I Cohen; Tzipora C Falik-Zaccai
Journal:  J Adolesc Health       Date:  2004-08       Impact factor: 5.012

10.  Conditional loss of PTEN leads to precocious development and neoplasia in the mammary gland.

Authors:  Gang Li; Gertraud W Robinson; Ralf Lesche; Hilda Martinez-Diaz; Zhaorong Jiang; Nora Rozengurt; Kay-Uwe Wagner; De-Chang Wu; Timothy F Lane; Xin Liu; Lothar Hennighausen; Hong Wu
Journal:  Development       Date:  2002-09       Impact factor: 6.868

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  1 in total

1.  Genetic linkage analysis in the presence of germline mosaicism.

Authors:  Omer Weissbrod; Dan Geiger
Journal:  Stat Appl Genet Mol Biol       Date:  2011-10-04
  1 in total

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