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
Top Mucopolysaccharidosis type vii Doctors on Curofy
Top doctors who continously share their opinions on Mucopolysaccharidosis type viiSuper Specialist in Reproductive Endocrinology
BHASKARA HOSPITAL
OBSTETRICIAN &GYNECOLOGIST
Kakatiya Medical College
M.D ( OB&GY )
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
ARPAN HOSPITAL
M.B.B.S., DFW, Dip. G O.
NARCHI
Dip. G. O.
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