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4 Best Doctors for Down syndrome in Okara

Dr. Sidra Yoosannaf

Pediatrician

MBBS, FCPS (Pediatrics), F.C.P.S.

1 Years Experience
100% (2) Satisfied Satisfied

Dr. Sidra Yoosannaf

Pediatrician

MBBS, FCPS (Pediatrics), F.C.P.S.

Dr. Abdur Rahman Ahmad

Pediatrician, Neonatologist

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

Under 15 Min Wait Time
6 Years Experience
100% (7) Satisfied Satisfied

Dr. Abdur Rahman Ahmad

Pediatrician, Neonatologist

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

Under 15 Min Wait Time
6 Years Experience

Dr. Sajid Majeed

Pediatrician

MBBS, FCPS

Dr. Sajid Majeed

Pediatrician

MBBS, FCPS

Dr. Hafiz Muhammad Yousaf

Pediatrician

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

2 Years Experience

Dr. Hafiz Muhammad Yousaf

Pediatrician

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

2 Years Experience
Yousaf Children Clinic (Faisalabad 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 Okara?

2 best doctors for down syndrome in Okara are:

  • Dr. Abdur Rahman Ahmad
  • Dr. Sidra Yoosannaf

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

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

The fee for the top doctors for Down syndrome in Okara is 500. 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 Okara 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.