A Case of Pfeiffer Syndrome with Hydrocephalus and Multiple Congenital Anomalies

Pfeiffer syndrome is one of a rare form of craniosynostosis syndrome, showing variable degree of craniosynostosis, midface hypoplasia, broad thumbs and toes and syndactyly. This is transmitted in autosomal dominant pattern and known to be related to mutations in FGFR (Fibroblast Growth Factor Receptor) 1 or FGFR 2. We experience a case of newborn Pfeiffer syndrome type 3 who had multiple facial anomalies, thumbs and great toes anomalies, ankylosis of radius and ulnar and hydrocephalus.

Resurfacing of the hand using free temporoparietal fascial flap

No abstract available.

Reconstruction of extensive scalp defect using free latissimus dorsi muscle flap

No abstract available.