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

noack syndrome
type v acrocephalosyndactyly
acrocephalosyndactyly type v
MainRecentTopDoctors

Top Pfeiffer syndrome Doctors on Curofy

Top doctors who continously share their opinions on Pfeiffer syndrome
Bangalore
877 followers

General Hospital Kanakapur

Md Pediatrics

MD Pediatrics

pediatrics

User Languages
Speaks English, Hindi, Kannada
kolkata
1142 followers
User Languages
Speaks English
Kurukshetra
2002 followers

Distt. Red Cross Society Bhawan

Honorary Medical Officer

SPMC, Bikaner

MBBS

User Languages
Speaks English
Hardoi
689 followers

Occupational Health Center

Medical Superintendent

King George's Medical University Lucknow

M.B.B.S

User Languages
Speaks English, Hindi
Theni
44 followers

Government Theni Medical College

mbbs intern

User Languages
Speaks English