Phenylketonuria
An autonomic recessive genetic disorder characterized by the body's inability to metabolize and utilize the amino acid phenylalanine, resulting in mental retardation, behavioral and movement problems, seizures, and developmental delays.
Disease Alternative Name
Recent Cases of Phenylketonuria
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Top doctors who continously share their opinions on PhenylketonuriaNational Institute of Medical Science
Md Paediatrics
National Institute of Medical Science
MD pediatrics

Super Specialist in Reproductive Endocrinology

Index Medical College
Professor & Hod
MGM Medical College, Indore
MBBS,MS ( ANATOMY)

Self Emploid(private Clinic)
Morbi
Shri M P Shah Medical College Jamnagar
M B B S

Private Practise
Md

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How would you describe the current understanding of autism in Indian population?
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Tibial aplasia and prosthetic Leg restoration. *Chief Complaints* Due to congenital anomalies she walks with abnormal gait patterns. *History* When she was born 28 years ago with such congenital anomalies. Her parents never thought that their 5th girl child would be the same as others 4 . But she had different problems with tibial aplasia and others 4 having complex syndactyly in both hands. Same as their father having complex syndactyly. *Vitals* Unable to perform activities of daily living. *Physical Examination* Problem with walking and gripping and grasping. *Management* 28 years old girl looking for Prosthetics management for tibial aplasia. Our team takes measurements and casting for Prosthetic Leg restoration. Now she walks comfortably with a new prosthetic Leg.
Dr. Narendra Kumar4 Likes2 Answers Which of the following approaches have you found effective when treating autistic patients in dental practice?
Dental-Insights2 Likes1 Answer
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