Literature DB >> 7401139

A digitopalatal syndrome with associated anomalies of the heart, face, and skeleton.

R E Stevenson, H A Taylor, O M Burton, H B Hearn.   

Abstract

A syndrome of multiple anomalies associated with growth failure and delayed development is described. The facies appear distinctive with globular head, prominence of the eyes, hypertelorism, cleft palate, micrognathia, and abnormal pinnae. Other features include vertebral and costal anomalies, cardiac defects, and a peculiar malformation of the hands. At least five other cases of this condition, all occurring in males, may be found in medical reports. The finding of incomplete expression in three maternal relatives of our patient provides evidence for a genetic cause.

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Year:  1980        PMID: 7401139      PMCID: PMC1048557          DOI: 10.1136/jmg.17.3.238

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


  6 in total

1.  Rachelefsky GS, Flynt JW Jr,+FLYNT JW JR, Ebbin AJ, Wilson MG, Banister P, Dafoe C, Smith ES, Miller J:Possible teratogenicity of tricyclic antidepressants.

Authors: 
Journal:  Lancet       Date:  1972-04-15       Impact factor: 79.321

2.  The William Allan Memorial Award Lecture: Genetic nosology: three approaches.

Authors:  V A McKusick
Journal:  Am J Hum Genet       Date:  1978-03       Impact factor: 11.025

3.  [The Pierre Robin syndrome: unusual associated developmental defects].

Authors:  W Holthusen
Journal:  Ann Radiol (Paris)       Date:  1972 Mar-Apr

4.  Limb deformities: possible association with drugs.

Authors:  R Freeman
Journal:  Med J Aust       Date:  1972-03-18       Impact factor: 7.738

5.  Glossoptotic hypoxia and micrognathia--the Pierre Robin syndrome reviewed. Early recognition and prompt surgical treatment is important for survival.

Authors:  P B Farnsworth; P T Pacik
Journal:  Clin Pediatr (Phila)       Date:  1971-10       Impact factor: 1.168

6.  Cleft palate and accessory metacarpal of index finger syndrome: possible familial occurrence.

Authors:  M Gewitz; R Dinwiddie; T Yuille; F Hill; C O Carter
Journal:  J Med Genet       Date:  1978-04       Impact factor: 6.318

  6 in total
  3 in total

1.  A male infant with the Catel-Manzke syndrome and dislocatable knees.

Authors:  E M Thompson; R M Winter; M J Williams
Journal:  J Med Genet       Date:  1986-06       Impact factor: 6.318

2.  Homozygous and compound-heterozygous mutations in TGDS cause Catel-Manzke syndrome.

Authors:  Nadja Ehmke; Almuth Caliebe; Rainer Koenig; Sarina G Kant; Zornitza Stark; Valérie Cormier-Daire; Dagmar Wieczorek; Gabriele Gillessen-Kaesbach; Kirstin Hoff; Amit Kawalia; Holger Thiele; Janine Altmüller; Björn Fischer-Zirnsak; Alexej Knaus; Na Zhu; Verena Heinrich; Celine Huber; Izabela Harabula; Malte Spielmann; Denise Horn; Uwe Kornak; Jochen Hecht; Peter M Krawitz; Peter Nürnberg; Reiner Siebert; Hermann Manzke; Stefan Mundlos
Journal:  Am J Hum Genet       Date:  2014-12-04       Impact factor: 11.025

3.  Pierre Robin sequence and hyperphalangy--a genetic entity (Catel-Manzke syndrome).

Authors:  E Brude
Journal:  Eur J Pediatr       Date:  1984-08       Impact factor: 3.183

  3 in total

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