Cleft lip and cleft palate closure in 13 month-old female with epidermolysis bullosa
JOURNAL OF CRANIOFACIAL SURGERY, vol.16, no.5, pp.843-847, 2005 (SCI-Expanded, Scopus)
- Publication Type: Article / Article
- Volume: 16 Issue: 5
- Publication Date: 2005
- Doi Number: 10.1097/01.scs.0000168768.40862.c5
- Journal Name: JOURNAL OF CRANIOFACIAL SURGERY
- Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus
- Page Numbers: pp.843-847
- Hacettepe University Affiliated: Yes
Abstract
Skin blistering and fragility are hallmarks of the rare hereditary disease called Epidemolysis Bullosa, affecting mainly the skin but also all mucocutaneous layers and sometimes the aero-digestive tract. Orofacial clefts are among the most common structural birth defects in humans, seen about 2 cases per 1000 births. This case report illustrates the closure of cleft lip and cleft palate in 13 month female with epidermolysis bullosa.