A Case of Split Hand Split Foot Anomaly.
- Author:
Mi Do LEE
1
;
Byung Moon AHN
;
Moo Young SONG
;
Eun Ryoung KIM
;
Mi Wook JIN
;
Il Soo KIM
Author Information
1. Department of Pediatrics, Sung-Ae General Hospital, Seoul, Korea.
- Publication Type:Case Report
- Keywords:
Split hand;
Split foot;
Chromosomal abnomality;
t(7p:14q)
- MeSH:
Fingers;
Foot*;
Hand*;
Humans;
Infant, Newborn;
Iris;
Karyotype;
Male;
Syndactyly;
Toes
- From:Journal of the Korean Pediatric Society
1999;42(7):1008-1013
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
We experienced a case of split hand split foot(SHSF) anomaly in a male neonate who had a deficiency of the middle finger, syndactyly of the 1st and 2nd finger and a deep median cleft in both hands. He also had a deep median cleft between 2nd and 3rd toe, syndactyly of the 1st and 2nd, 3rd and 4th toe without deficiency of the middle toe in both feet. SHSF anomaly may occur either isolated or associated with other anomalies. In this case, it occurd sporadically without family history and showed an isolated type without any other specific anomalies except both posterior iris synechiae. The karyotype of patient showed 46,XY,t(7p:14q) which has not been reported yet. We reported the case with the review of the associated literatures.
