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3 Best Doctors for Down syndrome in Muzaffargarh

Best Doctor for Down syndrome in Muzaffargarh - Dr. Abrar Hussain Shah

Dr. Abrar Hussain Shah

Pediatrician

M.B.B.S., F.C.P.S.

11 Years Experience

Dr. Abrar Hussain Shah

Pediatrician

M.B.B.S., F.C.P.S.

11 Years Experience
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Doctors Clinic (Muzaffargarh) (Alipur Road)
Hassan Clinic (Muzaffargarh) (Jhang Road)
Best Doctor for Down syndrome in Muzaffargarh - Dr. Yasir Aziz

Dr. Yasir Aziz

Pediatrician

M.B.B.S., F.C.P.S.

Under 15 Min Wait Time
5 Years Experience
91% (13) Satisfied Satisfied

Dr. Yasir Aziz

Pediatrician

M.B.B.S., F.C.P.S.

Under 15 Min Wait Time
5 Years Experience
91% (13) Satisfied Patients
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Call Helpline
Aziz Clinic (Muzaffargarh) (Alipur Road)
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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 Muzaffargarh?

3 best doctors for down syndrome in Muzaffargarh are:

  • Dr. Muhammad Yousuf
  • Dr. Yasir Aziz
  • Dr. Abrar Hussain Shah

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

Click here to book an appointment with top doctors for Down syndrome in Muzaffargarh. Or, you can also call at 04238900939 from 9AM to 11PM to book your appointment.

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

The fee for the top doctors for Down syndrome in Muzaffargarh is 2000. 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 Muzaffargarh 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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