Abstract
Eighty two cases of dwarfism of genetic etiology are described of 1100 cases referred to a specialised genetic clinic over 2 years. Short limb dwarfism (33 cases) formed the maximum number followed by chromosomal anomalies (25 cases). Eleven cases of genetic syndromes and 12 cases with metabolic disorders had short stature.
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Fairbank T: Dysplasia epiphysialis multiplex.Brit J Surg 34: 225, 1947
McKusick VA, Milch RA: The clinical behaviour of genetic diseases, selected aspects.Clin Orthop 33: 22, 1964
McKusick VA, Scott CI: The nomenclature of skeletal dysplasias.J Bone Jt Surg 53A: 978, 1971
Rubin P: Dynamic classification of bone dysplasias The Year Book Medical Publishers. Inc. Chicago, 1964
Scott CI Jr: The genetics of Short Stature,Prog Med Gen 7: 243, 1972
Frasier SD: Growth disorders in children,Pediatr Clin N Am 26: 1, 1979
Rimoin DL, Horton WA: Short stature Part I and II.J Pediatr 92:523, 697, 1978
Swanson AB: Classification system for congenital limb defects, in CIBA Symposium on congenttal limb defects.CIBA GEIGY Corp. 33: 4, 1982
Davies RW, Fairbank TJ: The mucopolysaccharidosis. In:Fairbank Atlas of general affections of skeleton, Second Ed; Churchill Livingstone, Edinburgh, London and New York, 1976 p 166
Phadke MA, Mutalik GS, Sainani GS: A study of dwarfism with special reference to chromosomal aberrations.Indian Pediatr 15: 409, 1978
Wadia RS, Shirole DB, Deshpande N: Genetic and diagnostic aspects of shortness of statute,Indian Pediatr 10: 577, 1973
Bharucha BA, Savliwala AS, Koppikar GV, Kumta NB: Camptomelic dwarfism syndrome, A case report.J Post Grad Med 29: 268, 1983
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Joshi, R.M., Bharucha, B.A., Kumta, N.B. et al. Genetics of congenital dwarfism. Indian J Pediatr 52, 545–547 (1985). https://doi.org/10.1007/BF02751034
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DOI: https://doi.org/10.1007/BF02751034