HealthCareMagic is now Ask A Doctor - 24x7 | https://www.askadoctor24x7.com

Get your health question answered instantly from our pool of 18000+ doctors from over 80 specialties
159 Doctors Online

By proceeding, I accept the Terms and Conditions

Dr. Andrew Rynne
MD
Dr. Andrew Rynne

Family Physician

Exp 50 years

HCM Blog Instant Access to Doctors
HCM BlogQuestions Answered
HCM Blog Satisfaction

Details About Congenital Adrenal Hyperplasia

is CAH treatment available well in India? How difficult is the life of a CAH affected baby girl initially and for the rest of the life?
Sat, 10 Sep 2011
Report Abuse
  User's Response
's  Response
Hi!
CAH treatment is available with most of the pediatric centres. The best one told to me is DR. Vageesh Ayyar from St. John's Hospital, ( as I am in bangalore) . child has to take tablet for entire life. for girl, its lesser complex than boy. Its not difficult life for them, but, some cases need constant hospitalisation. (salt water type CAH). It all depend on how we deal it . Our support for child wins the battle. My baby is doing well.
Dr Ayyar - Endocryanologist - availalable on Tue, Friday from 9 to 12 (50 Rs for normal or 300 rs for special) evening opd - 350 rs (wed,sat) you can call up and take an appointment ( not on the same day)
Dr. Vageesh is highly respected dr and private pediatricians and surgeons have sent me to him. he is humble and perfect in his work. He tells blood tests every three months that decided the dose of the tablet. That's it. St. Johns is not private clinic, so the pains of big hospital are there, but its worth for dr and your child.
pediatric surgeon, genetic dr.,councellor and all staff helped me a lot. Your child can become part of their group so that support is provided. But, I feel, its absolutely ok thing, unless, we take it like that. Doctors really help us to make things normal.
Orthopaedic Surgeon Dr. Aashish Raghu's  Response
Welcome to Healthcare Magic
Congenital Adrenal Hyperplasia is a disorder of enzyme deficiency in the adrenal glands. The main treatment will be steroid replacement which depends on the type of CAH and which enzymes are deficient. You need to consult an Endocrinologist and get tested and then the right treatment may be given.
I find this answer helpful
General & Family Physician Dr. Jitender Chauhan's  Response
Hello, welcome to Healthcaremagic. Yes treatment of CAH or congenital adrenal hyperplasia is available in India. Depending on the enzymes absent in your child, she would require administration of steroids for normal body function. If the treatment is done in a good way by carefull monitoring and administration of steroids you child can lead a very good life both initially and later part of life. Wish her good health.
I find this answer helpful

Note: For further queries related to your child health, Talk to a Pediatrician. Click here to Book a Consultation.
Disclaimer: These answers are for your information only and not intended to replace your relationship with your treating physician.
This is a short, free answer. For a more detailed, immediate answer, try our premium service [Sample answer]
Share on
 

Related questions you may be interested in


Recent questions on Adrenal gland disorder


Loading Online Doctors....
Details About Congenital Adrenal Hyperplasia

Hi! CAH treatment is available with most of the pediatric centres. The best one told to me is DR. Vageesh Ayyar from St. John s Hospital, ( as I am in bangalore) . child has to take tablet for entire life. for girl, its lesser complex than boy. Its not difficult life for them, but, some cases need constant hospitalisation. (salt water type CAH). It all depend on how we deal it . Our support for child wins the battle. My baby is doing well. Dr Ayyar - Endocryanologist - availalable on Tue, Friday from 9 to 12 (50 Rs for normal or 300 rs for special) evening opd - 350 rs (wed,sat) you can call up and take an appointment ( not on the same day) Dr. Vageesh is highly respected dr and private pediatricians and surgeons have sent me to him. he is humble and perfect in his work. He tells blood tests every three months that decided the dose of the tablet. That s it. St. Johns is not private clinic, so the pains of big hospital are there, but its worth for dr and your child. pediatric surgeon, genetic dr.,councellor and all staff helped me a lot. Your child can become part of their group so that support is provided. But, I feel, its absolutely ok thing, unless, we take it like that. Doctors really help us to make things normal.