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Pediatrics and Clinical Genetics
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About Me

I strive to create a warm, kid-friendly environment where children feel safe and cared for. My approach focuses on building trust with families while providing comprehensive, personalized care. Every child is unique, and I aim to support their health and development with compassion, clear communication, and a commitment to their overall well-being

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4.9+ 

Rated Online

5+ Years

Exp Pediatrics

92%

Parents Recommend

Dr. Nemmani Laxmi Kaveri

Pediatrics and Clinical Genetics

MBBS : Gandhi Medical College, Secunderabad
DNB Pediatrics : Rainbow Children’s Hospital, Banjara Hills, Hyderabad
Fellowship in Pediatric Genetics : Indira Gandhi Institute of Child Health

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Experience

  • 5 Years

Expertise

  • Clinical Genetics

  • Prenatal Counselling

Services Offered

  • General health check-ups

  • Vaccination

  • Nutritional counseling

  • Growth and development check

  • Management of common childhood illnesses

  • Prenatal counselling

  • Genetic counselling

Languages Spoken

  • English, Hindi, Kannada, Telugu

Please call Healthland Clinics to book your slot (+919364097115).

Meet our Specialists

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Dr. Anand Patil

Pediatrician and Neonatologist

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Dr. Obul Reddy

Pediatrician

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Dr. Tejaswi Chandra

Pediatrician and Pediatric Pulmonologist

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Dr. Nemmani Kaveri

Pediatrician and Clinical Geneticist

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Dr. Harish Nayak

Pediatric Ophthalmologist

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Dr. Premila Naidu

Pediatric Dentist

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Dr. Devesh Bhaskar Yerrapragada

General Paediatrics, Behaviourial Paediatrics

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Dr. Akash

Dermatologist

Hospital Care Interaction

Frequently Asked Questions

1. What is pediatric genetics?


Pediatric genetics is a specialized field that helps identify and understand genetic conditions that may affect a child’s growth, development, health, or inherited traits.

A pediatric genetic evaluation may help:

  • Understand developmental or medical concerns

  • Identify inherited conditions

  • Explain the cause of certain symptoms or delays

  • Guide treatment, monitoring, and long-term care

  • Assess risks for future pregnancies or family members

At HealthLand, our approach to pediatric genetics combines advanced clinical expertise with compassionate family-centered care, helping parents navigate complex concerns with clarity, sensitivity, and support.


2. When should my child see a pediatric geneticist?


A pediatric genetic consultation may be recommended if your child has:

  • Developmental delays or autism spectrum concerns

  • Learning difficulties or intellectual disability

  • Recurrent unexplained medical problems

  • Unusual physical features or growth patterns

  • Congenital anomalies or birth defects

  • Seizures without a clear cause

  • Metabolic or neuromuscular concerns

  • A strong family history of inherited disorders

Sometimes genetics evaluation is advised even when symptoms are subtle, especially if multiple developmental or medical concerns are present together.

At HealthLand, evaluations are conducted thoughtfully and sensitively, with a focus on helping families understand the “why” behind a child’s health concerns.


3. What happens during a pediatric genetics consultation?


A pediatric genetics consultation usually involves:

  • A detailed medical and developmental history

  • Review of family history across generations

  • Physical and developmental assessment of the child

  • Discussion about possible genetic conditions or testing options

If needed, the geneticist may recommend specific investigations such as blood tests, chromosome studies, or advanced genetic testing.

At HealthLand, consultations are designed to be informative, reassuring, and family-friendly, ensuring parents have the time and guidance needed to make informed decisions.


4. What is genetic testing in children?


Genetic testing analyzes a child’s genes or chromosomes to help identify conditions linked to inherited or spontaneous genetic changes.

Testing may help:

  • Confirm or rule out certain diagnoses

  • Guide medical treatment and therapies

  • Predict associated health risks

  • Support developmental planning and long-term care

Not every child requires genetic testing, and the type of test recommended depends on the child’s symptoms and clinical history.

At HealthLand, we help families understand the purpose, benefits, limitations, and implications of testing before proceeding.


5. Is genetic testing painful or risky for children?


Most genetic tests are simple and low risk. Many involve only:

  • A blood sample

  • A cheek swab

  • Occasionally urine or saliva samples

The testing process itself is generally safe. However, because genetic results can sometimes feel emotionally overwhelming, counselling and clear communication are an important part of the process.

At HealthLand, we ensure families receive compassionate guidance and support at every step, from evaluation to understanding results.


6. Can genetic conditions be treated in children?


Not all genetic conditions can be cured, but many can be managed effectively with early diagnosis, medical care, therapies, nutritional support, and developmental interventions.

Early identification can often:

  • Improve long-term outcomes

  • Help prevent complications

  • Support developmental progress

  • Enable personalized treatment planning

At HealthLand, pediatric genetics works closely with multidisciplinary specialists to provide coordinated care tailored to the child’s unique needs.


7. Are genetic conditions always inherited from parents?


Not always. Some genetic conditions are inherited, while others occur due to new genetic changes that happen spontaneously during development.

A child may have a genetic condition even if there is no known family history.

This is why genetics evaluation can sometimes provide answers even in families with no prior medical concerns.


At HealthLand, our specialists help families understand inheritance patterns, recurrence risks, and future family planning considerations with empathy and clarity.


8. Can genetics help identify the cause of developmental delay or autism?


In some children, genetic evaluation may help identify an underlying reason for developmental delays, autism spectrum disorder, intellectual disability, or certain behavioural and neurological conditions.

While not every child will have a genetic diagnosis, identifying an underlying cause can:

  • Guide therapy and medical care

  • Improve long-term planning

  • Help families better understand the child’s needs

  • Provide clarity regarding future risks or expectations

At HealthLand, genetic evaluations are integrated into a holistic developmental care approach focused on supporting both the child and family.


9. Should siblings or parents also undergo genetic testing?


In some situations, testing other family members may help:

  • Clarify inheritance patterns

  • Confirm a diagnosis

  • Assess risks for future pregnancies

  • Identify related health concerns in relatives

The need for family testing depends on the child’s diagnosis and the type of genetic condition suspected.

At HealthLand, genetic counselling helps families understand when additional testing may or may not be beneficial.


10. Does a referral for genetic evaluation mean my child has a serious condition?


Not necessarily. Children may be referred for genetics evaluation for a wide range of reasons — including mild developmental concerns, growth differences, learning challenges, or simply to rule out underlying conditions.

A genetics consultation is often part of a comprehensive effort to better understand a child’s health and development.


At HealthLand, we approach every child with sensitivity, respect, and individualized care, ensuring families feel supported rather than overwhelmed throughout the process.

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