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Chapter-21 Genetic and Congenital Disorders

BOOK TITLE: Partha’s Comprehensive Manual for Pediatric and Adolescent Practice

Author
1. Rai Ashok
2. R Remesh Kumar
3. Masand Rupesh
4. Gambhir Poonam Singh
ISBN
9789389776034
DOI
10.5005/jp/books/18348_23
Edition
1/e
Publishing Year
2020
Pages
25
Author Affiliations
1. Apollo Varanasi and Kilkari Institute of Child Health; Indian Institute of Cerebral Palsy and Handicapped Children, Varanasi, Uttar Pradesh, India, Varanasi, Uttar Pradesh, India, Surya Superspecialty Hospital, Varanasi, Kilkari Institute of Child Health, Varanasi; Indian Institute of Cerebral Palsy and Handicapped Children, Varanasi; Heritage Institute of Medical Sciences, Varanasi, Uttar Pradesh, India, Surya Super Speciality Hospital and Kilkari Institute of Child Health, Varanasi; Indian Institute of Cerebral Palsy and Handicapped Children, Varanasi, Uttar Pradesh, India, Surya Super Speciality Hospital, Varanasi, Kilkari Institute of Child Health Private Limited, Varanasi; Indian Institute of Cerebral Palsy and Handicapped Children, Varanasi; Heritage Institute of Medical Sciences, Varanasi, Uttar Pradesh, India, Heritage Institute of Medical Sciences Varanasi; Indian Institute of Cerebral Palsy and Handicapped Children, Varanasi, Uttar Pradesh, India, Clinical Genetics; Allergy and Clinical Immunology;
2. Apollo Adlux Hospital, Cochin, Kerala India; Central IAP 2018 and 2019, Apollo Adlux Hospital, Kochi, Kerala, India, Apollo Adlux Hospital, Cochin, Kerala, India, Apollo Adlux Hospital, Ernakulam, Kerala, India, IAP President 2022, NSS Medical Mission Superspecialty, Hospital, Pandalam, Kerala
3. National Institute of Medical Sciences and Research, Jaipur, Rajasthan, India, National Institute of Medical Science and Research, Jaipur, Rajasthan, India
4. Vardaan Genetic and Diagnostic Centre, Regency Hospital, Kanpur, Uttar Pradesh, India
Chapter keywords
Genetic disorder, congenital disorder, duchenne muscular dystrophy, Down Syndrome, Fragile X syndrome, neural tube defect, Turner syndrome, neurofibromatosis, achondroplasia, tuberous sclerosis complex, craniosynostosis, spinal muscular atrophy

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