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2 Best Doctors for Down syndrome in Jhang

Best Doctor for Down syndrome in Jhang - Dr. Muhammad Bilal Mazhar

Dr. Muhammad Bilal Mazhar

Pediatrician, Pediatric Nutritionist, Neonatologist

M.B.B.S, FCPS, MRCPCH-II, PGPN (USA)

Under 15 Min Wait Time
6 Years Experience
100% (128) Satisfied Satisfied

Dr. Muhammad Bilal Mazhar

Pediatrician, Pediatric Nutritionist, Neonatologist

M.B.B.S, FCPS, MRCPCH-II, PGPN (USA)

Under 15 Min Wait Time
6 Years Experience
100% (128) Satisfied Patients
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PMC Verified
Best Doctor for Down syndrome in Jhang - Dr. Asim Umar

Dr. Asim Umar

Pediatrician

MBBS, FCPS (Pediatrics)

15 - 30 Min Wait Time
8 Years Experience
50% (2) Satisfied Satisfied

Dr. Asim Umar

Pediatrician

MBBS, FCPS (Pediatrics)

15 - 30 Min Wait Time
8 Years Experience
50% (2) Satisfied Patients
View Profile
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Shakir Hospital (Bhawana Painsra Road) Rs. 700
Available today
Rs. 700
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What is Down syndrome?

Down syndrome (DS or DNS), also known as trisomy 21, is a genetic disorder caused by the presence of all or part of a third copy of chromosome 21. It is typically associated with physical growth delays, characteristic facial features, and mild to moderate intellectual disability.

Frequently Asked Questions

Who is the best doctor for down syndrome in Jhang?

2 best doctors for down syndrome in Jhang are:

  • Dr. Muhammad Bilal Mazhar
  • Dr. Asim Umar

How can I book an appointment with a doctor for Down syndrome in Jhang?

Click here to book an appointment with top doctors for Down syndrome in Jhang. Or, you can also call at 0415068065 from 9AM to 11PM to book your appointment.

What is the fee range of the best doctors for Down syndrome in Jhang?

The fee for the top doctors for Down syndrome in Jhang ranges from Rs. 700 to 1,000. You can pay at reception when you visit the doctor.

Are there any additional charges to book an appointment with doctors for Down syndrome in Jhang through oladoc?

There are no additional charges when you book through oladoc.

What is Down syndrome?

Down syndrome (DS or DNS), also known as trisomy 21, is a genetic disorder caused by the presence of all or part of a third copy of chromosome 21. It is typically associated with physical growth delays, characteristic facial features, and mild to moderate intellectual disability.

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