Indian Journal of Human Genetics
Home Current Issue Archives Guidelines Subscriptions e-Alerts Login 
Users online: 43
Print this page  Email this page Small font sizeDefault font sizeIncrease font size
CASE REPORT
Year : 2012  |  Volume : 18  |  Issue : 3  |  Page : 376-378

Orofaciodigital syndrome type-VI (Varadi-Papp syndrome) with several Y-shaped metacarpals


1 Department of Paediatrics, Paediatric Unit, S. D. Hospital, Jhargram, India
2 Department of Radio-Diagnosis, Radiology Unit, Spandan Hospital, Medinipur, West Bengal, India

Correspondence Address:
Pulak R Mahato
Senior Medical Officer (Paediatrician), Sub-Divisional Hospital, Jhargram, Dist. Paschim Medinipur, West Bengal - 721 507
India
Login to access the Email id

Source of Support: None, Conflict of Interest: None


DOI: 10.4103/0971-6866.108053

Get Permissions

Orofaciodigital syndrome type-VI (Varadi-Papp Syndrome) is a rare autosomal recessive disorder characterized by variable orofacial anomalies, central polydactyly of the hands, and cerebellar dysgenesis (mainly hypoplasia or aplasia of vermis, rarely Dandy-Waker anomaly). Here a case of Varadi-Papp syndrome with recurrent episodic tachypnea-apnea, minimal orofacial features, several Y-shaped metacarpals, and cerebellar vermis hypoplasia, diagnosed in the neonatal age, is reported for the first time in Indian literature. The importance of early accurate diagnosis of this rare disease for proper genetic counseling and prenatal case detection of pregnancy at risk is also emphasized as the prognosis is poor in almost all cases.


[FULL TEXT] [PDF]*
Print this article     Email this article
 Next article
 Previous article
 Table of Contents

 Similar in PUBMED
   Search Pubmed for
   Search in Google Scholar for
 Related articles
 Citation Manager
 Access Statistics
 Reader Comments
 Email Alert *
 Add to My List *
 * Requires registration (Free)
 

 Article Access Statistics
    Viewed2123    
    Printed21    
    Emailed0    
    PDF Downloaded27    
    Comments [Add]    
    Cited by others 1    

Recommend this journal