Cardiofaciocutaneous syndrome: A rare entity
The cardiofaciocutaneous (CFC) syndrome is a condition of sporadic occurrence, with patients showing multiple congenital anomalies and mental retardation and characteristic dysmorphic features. We, thus, report a rare case of this syndrome in a 1-year-old child who presented with typical features of...
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Wolters Kluwer Medknow Publications
2012-01-01
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doaj-1e46aa46fe294a7bae6fae4061d369bd2020-11-24T23:22:12ZengWolters Kluwer Medknow PublicationsIndian Journal of Dermatology0019-51541998-36112012-01-0157429930110.4103/0019-5154.97677Cardiofaciocutaneous syndrome: A rare entityS PavithraH MallyaG S PaiThe cardiofaciocutaneous (CFC) syndrome is a condition of sporadic occurrence, with patients showing multiple congenital anomalies and mental retardation and characteristic dysmorphic features. We, thus, report a rare case of this syndrome in a 1-year-old child who presented with typical features of CFC syndrome.http://www.e-ijd.org/article.asp?issn=0019-5154;year=2012;volume=57;issue=4;spage=299;epage=301;aulast=PavithraAnomaliescardiofaciocutaneous syndromedefects |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
S Pavithra H Mallya G S Pai |
spellingShingle |
S Pavithra H Mallya G S Pai Cardiofaciocutaneous syndrome: A rare entity Indian Journal of Dermatology Anomalies cardiofaciocutaneous syndrome defects |
author_facet |
S Pavithra H Mallya G S Pai |
author_sort |
S Pavithra |
title |
Cardiofaciocutaneous syndrome: A rare entity |
title_short |
Cardiofaciocutaneous syndrome: A rare entity |
title_full |
Cardiofaciocutaneous syndrome: A rare entity |
title_fullStr |
Cardiofaciocutaneous syndrome: A rare entity |
title_full_unstemmed |
Cardiofaciocutaneous syndrome: A rare entity |
title_sort |
cardiofaciocutaneous syndrome: a rare entity |
publisher |
Wolters Kluwer Medknow Publications |
series |
Indian Journal of Dermatology |
issn |
0019-5154 1998-3611 |
publishDate |
2012-01-01 |
description |
The cardiofaciocutaneous (CFC) syndrome is a condition of sporadic occurrence, with patients showing multiple congenital anomalies and mental retardation and characteristic dysmorphic features. We, thus, report a rare case of this syndrome in a 1-year-old child who presented with typical features of CFC syndrome. |
topic |
Anomalies cardiofaciocutaneous syndrome defects |
url |
http://www.e-ijd.org/article.asp?issn=0019-5154;year=2012;volume=57;issue=4;spage=299;epage=301;aulast=Pavithra |
work_keys_str_mv |
AT spavithra cardiofaciocutaneoussyndromearareentity AT hmallya cardiofaciocutaneoussyndromearareentity AT gspai cardiofaciocutaneoussyndromearareentity |
_version_ |
1725568795341225984 |