Apert syndrome

An autosomal dominant inherited type of acrocephalosyndactyly caused by mutations in the FGFR2 gene. It is characterized by early closure of the sutures between the skull bones, bulging eyes, low-set ears, fusion of the second, third, and forth fingers, and fusion of the toes.

Disease Alternative Name

acrocephalosyndactyly type i
type i acrocephalosyndactyly
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Dhanbad
1817 followers

National Institute of Medical Science

Md Paediatrics

National Institute of Medical Science

MD pediatrics

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Srinagar Picture In BAITAB VALLEY PEHLGAM
466 followers

JLNM RAINAWARI

Consultant Pediatrics

GMC SRINAGAR

MD Pediatrics

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Bangalore
878 followers

General Hospital Kanakapur

Md Pediatrics

MD Pediatrics

pediatrics

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Davangere
522 followers

Jagadguru Jayadeva Murugarajendra Medical College

Retired Professor and Head Pediatrics

Jagadguru Jayadeva Murugarajendra Medical College

md,frcpch(uk),ficpcc(London),masp(usa),phd, fams ,fimsa.

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Patiala
1533 followers

Sangrur

Distt.Immunization Officer

Guru Gobind Singh Govt. Medical College, Faridkot

MBBS,DCH

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NAVJEEVAN NEONATAL AND CHILD CARE HOSPITAL SIRSA
643 followers

AADESH MEDICAL COLLEGE

Associate Professor HEAD OF UNIT PAEDIATRIC

Dr SN Medical College Jodhpur

MD PAEDS

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Speaks English, Hindi
Barpali
2564 followers

Self Employed. Now Doing My Practice

Pediatric Consultant

MKCG MCH

MBBS and MD (pediatrics)

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Meerut
242 followers

LLRM

Senior Resident

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Kurukshetra
2001 followers

Distt. Red Cross Society Bhawan

Honorary Medical Officer

SPMC, Bikaner

MBBS

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JLNMCH, Bhagalpur
45 followers

Dr RML Hospital & PGIMER New Delhi

Senior Resident (Pediatrics)

DMCH

MD (Pediatrics)

User Languages
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