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4 Best Doctors for Down syndrome in Sialkot

PMC Verified

Dr. Syed Mehboob Gillani

Pediatrician, Neonatologist

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

Under 15 Min Wait Time
4 Years Experience
100% (12) Satisfied Satisfied

Dr. Syed Mehboob Gillani

Pediatrician, Neonatologist

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

Under 15 Min Wait Time
4 Years Experience
PMC Verified

Dr. Salman Arshad

Pediatrician

M.B.B.S., F.C.P.S. (Pediatrics)

8 Years Experience

Dr. Salman Arshad

Pediatrician

M.B.B.S., F.C.P.S. (Pediatrics)

8 Years Experience

Dr. Tahniyat Huq

Pediatrician

MBBS, MCPS (Pediatrics)

15 - 30 Min Wait Time
5 Years Experience
100% (3) Satisfied Satisfied

Dr. Tahniyat Huq

Pediatrician

MBBS, MCPS (Pediatrics)

15 - 30 Min Wait Time
5 Years Experience

Dr. Asad Amaar

Pediatrician

MBBS

Dr. Asad Amaar

Pediatrician

MBBS

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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 Sialkot?

3 best doctors for down syndrome in Sialkot are:

  • Dr. Syed Mehboob Gillani
  • Dr. Tahniyat Huq
  • Dr. Salman Arshad

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

Click here to book an appointment with top doctors for Down syndrome in Sialkot. 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 Sialkot?

The fee for the top doctors for Down syndrome in Sialkot is 1500. 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 Sialkot 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.