Literature DB >> 7815445

Cleft hand/foot: clinical and developmental aspects.

P W Buss1.   

Abstract

Isolated limb reduction defects occur in approximately 1 in 2000 live births within which central ray anomalies are an important subgroup. Most affected persons have mild or moderate functional impairment. Considerable psychological morbidity may also occur. While there have been major strides forwards in our understanding of vertebrate limb development, the mechanisms responsible for central ray deformities remain poorly understood. Several case reports of central clefting anomalies associated with chromosomal rearrangements or interstitial deletions of 7q21.2-q21.3 suggest that this chromosomal region is important for limb development.

Entities:  

Mesh:

Year:  1994        PMID: 7815445      PMCID: PMC1050086          DOI: 10.1136/jmg.31.9.726

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  38 in total

1.  CRANIO-FACIAL DYSOSTOSIS AND MALFORMATIONS OF FEET.

Authors:  T J PATTERSON; A C STEVENSON
Journal:  J Med Genet       Date:  1964-12       Impact factor: 6.318

2.  Ectrodactyly--evidence in favour of a disturbed segregation in the offspring of affected males.

Authors:  A C STEVENSON; L M JENNINGS
Journal:  Ann Hum Genet       Date:  1960-04       Impact factor: 1.670

3.  Split-hand and split-foot deformity inherited as an autosomal recessive trait.

Authors:  I C Verma; R Joseph; S Bhargava; S Mehta
Journal:  Clin Genet       Date:  1976-01       Impact factor: 4.438

Review 4.  Mechanisms of limb development and malformation.

Authors:  L Wolpert
Journal:  Br Med Bull       Date:  1976-01       Impact factor: 4.291

5.  A problem for genetic counselling - split hand deformity.

Authors:  A E Emery
Journal:  Clin Genet       Date:  1977-08       Impact factor: 4.438

6.  Dominant ectrodactyly and possible germinal mosaicism.

Authors:  T J David
Journal:  J Med Genet       Date:  1972-09       Impact factor: 6.318

7.  Sonic hedgehog mediates the polarizing activity of the ZPA.

Authors:  R D Riddle; R L Johnson; E Laufer; C Tabin
Journal:  Cell       Date:  1993-12-31       Impact factor: 41.582

8.  Constrictive bands in the human.

Authors:  S S Gellis
Journal:  Birth Defects Orig Artic Ser       Date:  1977

9.  A mutation in the homeodomain of the human MSX2 gene in a family affected with autosomal dominant craniosynostosis.

Authors:  E W Jabs; U Müller; X Li; L Ma; W Luo; I S Haworth; I Klisak; R Sparkes; M L Warman; J B Mulliken
Journal:  Cell       Date:  1993-11-05       Impact factor: 41.582

Review 10.  Syndactylies and polydactylies: embryological overview and suggested classification.

Authors:  R M Winter; C Tickle
Journal:  Eur J Hum Genet       Date:  1993       Impact factor: 4.246

View more
  6 in total

Review 1.  Hidrotic ectodermal dysplasia of hair, teeth, and nails: case reports and review.

Authors:  L S Chitty; N Dennis; M Baraitser
Journal:  J Med Genet       Date:  1996-08       Impact factor: 6.318

2.  A case of atypical cleft hand - reported with ontogenetic review.

Authors:  Sujit Kumar Kundu; Hironmoy Roy; Abhijit Datta
Journal:  J Clin Diagn Res       Date:  2014-12-05

3.  Unilateral cleft hand with cleft foot.

Authors:  Asif Nazir Baba; Yasmeen J Bhat; Sheikh Mushtaq Ahmed; Abid Nazir
Journal:  Int J Health Sci (Qassim)       Date:  2009-07

4.  Pollicization of Middle Finger in a Cleft Hand Associated with Acrorenal Syndrome.

Authors:  Rajendra S Gujjalanavar; Marichamy R Muthukishore; R Jainath; Sathya Vamsi Krishna
Journal:  J Hand Microsurg       Date:  2020-04-28

5.  Twenty-four cases of the EEC syndrome: clinical presentation and management.

Authors:  P W Buss; H E Hughes; A Clarke
Journal:  J Med Genet       Date:  1995-09       Impact factor: 6.318

6.  Prenatal Diagnosis of Ectrodactyly in the First Trimester by Three-Dimensional Ultrasonography.

Authors:  Matthew J Blitz; Burton Rochelson
Journal:  AJP Rep       Date:  2016-03
  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.