Mucopolysaccharidosis type vii

A rare autosomal recessive lysosomal storage disease caused by deficiency of the enzyme N-acetylglucosamine-6-sulfatase. It is characterized by behavioral changes, sleep disturbances and mental developmental delays.

Disease Alternative Name

mps iii d
sanfilippo d
mucopolysaccharidosis type iiid
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Top Mucopolysaccharidosis type vii Doctors on Curofy

Top doctors who continously share their opinions on Mucopolysaccharidosis type vii
Surat
1189 followers

Super Specialist in Reproductive Endocrinology

User Languages
Speaks English
Hyderabad
2098 followers

BHASKARA HOSPITAL

OBSTETRICIAN &GYNECOLOGIST

Kakatiya Medical College

M.D ( OB&GY )

User Languages
Speaks Malyalam
VIJAYAWADA
255 followers

Dr.Pinnamaneni Siddhartha Institute of Medical Sciences and Research Foundation

M.B.B.S Student

Dr. Pinnamaneni Siddhartha Institute of Medical Sciences and Research Foundation

M.B.B.S

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Speaks English, Hindi, Telugu
Porbandar
1749 followers

ARPAN HOSPITAL

M.B.B.S., DFW, Dip. G O.

NARCHI

Dip. G. O.

User Languages
Speaks English, Gujarati, Hindi, Marathi

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