Literature DB >> 5006208

Genetic heterogeneity in the Waardenburg syndrome.

S Arias.   

Abstract

Waardenbury syndrome is divided into three groups: Type I, with dystopia; Type II, and "pseudo-Waardenburg" syndrome, without dystopia; the third has unilateral congenital ptosis. Using Waardenburg's original variables a, b and c, ratios a/b and c/a, Cotterman's L function, newly described indices X and Y and some phenotypic manifestations, a confident neat separation of each type can be obtained. New cases of all types and electron micrographs of the hair pigment anomaly are described.

Entities:  

Mesh:

Year:  1971        PMID: 5006208

Source DB:  PubMed          Journal:  Birth Defects Orig Artic Ser        ISSN: 0547-6844


  22 in total

1.  Probable loose linkage between the ABO locus and Waardenburg syndrome type I.

Authors:  S Arias; M Mota; A Yánez; M Bolivar
Journal:  Humangenetik       Date:  1975

2.  Analyses of loss-of-function mutations of the MITF gene suggest that haploinsufficiency is a cause of Waardenburg syndrome type 2A.

Authors:  Y Nobukuni; A Watanabe; K Takeda; H Skarka; M Tachibana
Journal:  Am J Hum Genet       Date:  1996-07       Impact factor: 11.025

3.  Multimodal Ultrawide-Field Imaging Features in Waardenburg Syndrome.

Authors:  Netan Choudhry; Rajesh C Rao
Journal:  Ophthalmic Surg Lasers Imaging Retina       Date:  2015-06       Impact factor: 1.300

4.  Waardenburg syndrome: A rare case with bilateral congenital cataract: An unusual entity.

Authors:  Nitin Vichare; N Bhargava
Journal:  Med J Armed Forces India       Date:  2012-12-01

5.  Waardenburg-like features with cataracts, small head size, joint abnormalities, hypogonadism, and osteosarcoma.

Authors:  D M Parry; A W Safyer; J J Mulvihill
Journal:  J Med Genet       Date:  1978-02       Impact factor: 6.318

Review 6.  The incidence of deafness is non-randomly distributed among families segregating for Waardenburg syndrome type 1 (WS1).

Authors:  R Morell; T B Friedman; J H Asher; L G Robbins
Journal:  J Med Genet       Date:  1997-06       Impact factor: 6.318

7.  Homozygosity in piebald trait.

Authors:  M A Hultén; M M Honeyman; A J Mayne; M J Tarlow
Journal:  J Med Genet       Date:  1987-09       Impact factor: 6.318

8.  Pigment distribution in Waardenburg's syndrome: a new hypothesis.

Authors:  T M Nork; Z M Shihab; R S Young; J Price
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  1986       Impact factor: 3.117

9.  Genetic mapping of X-linked albinism-deafness syndrome (ADFN) to Xq26.3-q27.I.

Authors:  Y Shiloh; G Litvak; Y Ziv; T Lehner; L Sandkuyl; M Hildesheimer; V Buchris; F P Cremers; P Szabo; B N White
Journal:  Am J Hum Genet       Date:  1990-07       Impact factor: 11.025

10.  Assignment of the locus for Waardenburg syndrome type I to human chromosome 2q37 and possible homology to the Splotch mouse.

Authors:  C Foy; V Newton; D Wellesley; R Harris; A P Read
Journal:  Am J Hum Genet       Date:  1990-06       Impact factor: 11.025

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