Pfeiffer syndrome
An autosomal dominant inherited type of acrocephalosyndactyly caused by mutations in the FGFR1 or FGFR2 genes. It is characterized by early closure of the sutures between the skull bones, bulging and wide-set eyes, broad thumbs, big toes, and partial syndactyly in the hands and toes.
Disease Alternative Name
Top Pfeiffer syndrome Doctors on Curofy
Top doctors who continously share their opinions on Pfeiffer syndrome
General Hospital Kanakapur
Md Pediatrics
MD Pediatrics
pediatrics
Distt. Red Cross Society Bhawan
Honorary Medical Officer
SPMC, Bikaner
MBBS
Occupational Health Center
Medical Superintendent
King George's Medical University Lucknow
M.B.B.S
Government Theni Medical College
mbbs intern
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