Experienced Doctors for Monosomy 1P36 Syndrome in Sangamner

1 Specialist(s)
Dr Snehal Shivaji Jagtap

Dr Snehal Shivaji Jagtap

Consultant Pediatrician and Neonatologist
Sangamner Experience: 3+ Yrs

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Doctors for Monosomy 1P36 Syndrome Treatment in Sangamner

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.

Symptoms such as facial dysmorphism, congenital anomalies and cardiomyopathy may affect daily activities when associated with monosomy 1p36 syndrome. Without appropriate medical attention, some conditions can progress or lead to additional health concerns.

At Medicover Hospitals in Sangamner, our monosomy 1p36 syndrome doctors (pediatricians) assess the condition and recommend suitable care based on the patient's symptoms, diagnosis, disease severity, and overall health. Treatment may vary depending on individual medical needs.

Our specialists provide care for patients who require initial treatment, follow-up support, or ongoing disease management. The aim is to control symptoms, address underlying health concerns where possible, and support better quality of life.

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Why Choose Our Doctors in Sangamner?

Our experienced pediatricians at Medicover Hospital, Sangamner, diagnoses and treats monosomy 1p36 syndrome using advanced medical facilities and a patient-focused approach.

Key Reasons to Choose Our Specialists

  • Experienced specialists providing expert care for cardiac, orthopedic, neurological, urological, and other specialised conditions
  • Doctors supported by 40 ICU beds and dedicated critical care services for managing complex cases
  • We provided the cardiac specialists with round-the-clock advanced cath lab support
  • Surgeons perform advanced procedures in modern operation theatres while adhering to strict safety standards
  • Emergency and trauma doctors backed by 24/7 diagnostic, radiology, and ambulance services
  • Dedicated surgical teams available round-the-clock for urgent and high-risk procedures
  • Patient-focused doctors delivering personalised treatment plans for safe recovery and better outcomes

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Frequently Asked Questions

1. Who provides treatment for monosomy 1p36 syndrome in Sangamner?

Treatment for monosomy 1p36 syndrome at Medicover Hospitals, Sangamner is provided by qualified pediatric specialists using advanced technology, evidence-based treatment plans, and patient-focused care for effective disease management.

2. What symptoms should I watch for in monosomy 1p36 syndrome?

Watch for symptoms such as facial dysmorphism, congenital anomalies and cardiomyopathy, as they may indicate monosomy 1p36 syndrome. If these symptoms continue or become more severe, consult a healthcare professional for further evaluation.

3. Which treatment is recommended for monosomy 1p36 syndrome?

The recommended treatment for monosomy 1p36 syndrome depends on factors such as the stage of the condition, symptoms, and overall health. At Medicover Hospitals in Sangamner, our pediatric specialists evaluate each patient and recommend the most suitable treatment plan.

4. When can I expect to recover from monosomy 1p36 syndrome?

The time needed to recover from monosomy 1p36 syndrome varies for each individual. Recovery is influenced by the severity of the disease, overall health, and how well the body responds to treatment.

5. How do I book a consultation for monosomy 1p36 syndrome in Sangamner?

Appointments can be booked online, by calling 040-68334455, or by visiting Medicover Hospitals in Sangamner. Our staff will guide you through the booking process and help schedule your consultation.

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