HOLT-ORAM SYNDROME: RARE CASE SERIES-Reference-Cited by-同舟云学术

HOLT-ORAM SYNDROME: RARE CASE SERIES

Published:2021-11-15 Issue: Volume: Page:46-47
ISSN:
Container-title:GLOBAL JOURNAL FOR RESEARCH ANALYSIS
language:en
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Author:

Reddy Muskula Mahendar¹,P Roshin¹,J Ajay²,Chetty Sanjeev³

Affiliation:

1. P.G. M.D. Paediatrics, Department of Paediatrics, Navodaya Medical college Hospital and Research Centre, Raichur 584101.

2. Associate professor, Department of Paediatrics, Navodaya Medical college Hospital and Research Centre, Raichur 584101.

3. Professor, Department of Paediatrics, Navodaya Medical college Hospital and Research Centre, Raichur 584101.

Abstract

The upper limb malformations in association with congenital heart defects occurring as autosomal dominant disorder are seen in Holt-Oram syndrome. It is a very rare disorder which can be detected with early prenatal ultrasound checkups. Here we are reporting two cases of holt-oram syndrome

Publisher

World Wide Journals

Reference7 articles.

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