Leading Monosomy 1P36 Syndrome Specialists in Warangal

1 Specialist(s)

Dr Ashritha Rao Komandla

Consultant Paediatrician

Warangal Experience: 3+ Yrs

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Doctors for Monosomy 1P36 Syndrome Treatment in Warangal

Monosomy 1p36 syndrome is a rare genetic condition people are born with, caused by a missing piece at the end of chromosome 1. That tiny loss can affect how a child grows and develops, leading to delays in learning and speech, low muscle tone, seizures, heart problems, and unique facial features. Symptoms vary from person to person.

People with monosomy 1p36 syndrome may notice symptoms such as facial dysmorphism, hearing loss and hypotonia. A medical evaluation can help determine the nature and severity of the condition and whether treatment or ongoing monitoring is needed.

At Medicover Hospitals in Warangal, our pediatricians evaluate patients with monosomy 1p36 syndrome and recommend care according to their clinical findings, medical history, and individual health requirements. Relevant diagnostic tests may be used when necessary to support treatment decisions.

Our medical team supports patients throughout their care, from initial assessment and treatment to follow-up and long-term management when required, with a focus on controlling symptoms and maintaining overall health.

Find Pediatricians for Monosomy 1p36 Syndrome Treatment Near You

Why Choose Our Doctors in Warangal?

For complete care in monosomy 1p36 syndrome, our experienced pediatricians in Warangal delivers accurate diagnosis and effective treatment. With advanced clinical expertise and modern medical support, our doctors ensure safe and compassionate care from initial consultation through recovery.

Key Reasons to Choose Our Specialists