Literature DB >> 27694333

Waardenburg-Shah Syndrome: a rare case in an Indian child.

Rajesh Pattebahadur1, Shipra Singhi2, Prafulla Kumar Maharana3.   

Abstract

A 7-year-old male child presented with a history of discolouration of right eye since birth. On examination visual acuity was 6/6 on Snellen's chart in both eyes; anterior segment was within normal limits except for the brilliant blue discolouration of the inferior quadrant and superior quadrant of right iris and left eye iris, respectively. Both eyes had a clear lens and fundus findings were within normal limits. A detailed history from parents revealed that the child had difficulty in hearing and slurring of speech. In addition, the child had repeated episodes of constipation with bilious vomiting during infancy for which a diagnosis of fungal sepsis with Hirschsprung's disease was made and the child had to undergo a mid-sigmoid loop colostomy for that. A diagnosis of Waardenburg--Shah Syndrome was made and the child was referred for hearing and speech rehabilitation. 2016 BMJ Publishing Group Ltd.

Entities:  

Mesh:

Year:  2016        PMID: 27694333      PMCID: PMC5051414          DOI: 10.1136/bcr-2016-216366

Source DB:  PubMed          Journal:  BMJ Case Rep        ISSN: 1757-790X


  7 in total

1.  Delayed presentation of children with Waardenburg syndrome.

Authors:  Mridula Mehta; Sumita Sethi; Neelam Pushker; Mandeep S Bajaj; Supriyo Ghose
Journal:  J Pediatr Ophthalmol Strabismus       Date:  2010 Nov-Dec       Impact factor: 1.402

2.  A new syndrome combining developmental anomalies of the eyelids, eyebrows and nose root with pigmentary defects of the iris and head hair and with congenital deafness.

Authors:  P J WAARDENBURG
Journal:  Am J Hum Genet       Date:  1951-09       Impact factor: 11.025

3.  Waardenburg syndrome: iris and choroidal hypopigmentation: findings on anterior and posterior segment imaging.

Authors:  Carol L Shields; Stephanie J Nickerson; Saad Al-Dahmash; Jerry A Shields
Journal:  JAMA Ophthalmol       Date:  2013-09       Impact factor: 7.389

4.  Waardenburg syndrome (WS) type I is caused by defects at multiple loci, one of which is near ALPP on chromosome 2: first report of the WS consortium.

Authors:  L A Farrer; K M Grundfast; J Amos; K S Arnos; J H Asher; P Beighton; S R Diehl; J Fex; C Foy; T B Friedman
Journal:  Am J Hum Genet       Date:  1992-05       Impact factor: 11.025

5.  Waardenburg syndrome--a case report.

Authors:  Yuvika Bansal; Parul Jain; Gaurav Goyal; Malvika Singh; Chittranjan Mishra
Journal:  Cont Lens Anterior Eye       Date:  2012-10-31       Impact factor: 3.077

Review 6.  Intestinal aganglionosis associated with the Waardenburg syndrome: report of two cases and review of the literature.

Authors:  Fumiaki Toki; Norio Suzuki; Ken Inoue; Makoto Suzuki; Kyoko Hirakata; Kyoko Nagai; Minoru Kuroiwa; James R Lupski; Yoshiaki Tsuchida
Journal:  Pediatr Surg Int       Date:  2003-12-23       Impact factor: 1.827

7.  Waardenburg Shah syndrome: A rare case from India.

Authors:  Meenakshi Wadhwani; Yogesh Kumar Gupta; Kulbhushan Gangwani
Journal:  Oman J Ophthalmol       Date:  2015 Jan-Apr
  7 in total
  1 in total

1.  Shah-Waardenburg syndrome: a case highlighting the importance of a holistic approach to assessing a child.

Authors:  Amogh Patil; Lanka Prathyusha; Muganagowda Patil
Journal:  BMJ Case Rep       Date:  2017-12-22
  1 in total

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