Expert Monosomy 1P36 Syndrome Specialists in Kurnool

1 Specialist(s)

Dr K Sindhura

Consultant Pediatrician and Neonatologist

Kurnool Experience: 5+ Yrs

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Doctors for Monosomy 1P36 Syndrome Treatment in Kurnool

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.

Monosomy 1P36 Syndrome may cause symptoms such as hearing loss, hypotonia and developmental delay. Depending on the condition and its severity, delayed medical care may result in persistent symptoms, progression of the disease, or related complications.

At Medicover Hospitals in Kurnool, our experienced doctors (pediatricians) provide evaluation and treatment for monosomy 1p36 syndrome. Where appropriate, our specialists use relevant diagnostic tests to understand the patient's condition and recommend treatment based on clinical findings and individual health needs.

From early evaluation to ongoing management, our specialists provide evidence-based care focused on controlling symptoms, managing the condition, reducing potential complications, and supporting the patient's overall well-being.

Find Pediatricians for Monosomy 1p36 Syndrome Treatment Near You

Why Choose Our Doctors in Kurnool?

For specialised care in monosomy 1p36 syndrome, our experienced pediatricians at Medicover Hospital, Kurnool, provides accurate diagnosis and personalised treatment. Our doctors are supported by modern technology, advanced specialities and a compassionate patient-centric approach for reliable outcomes.

Key Reasons to Choose Our Specialists