Top Abstract Purchase Related
Home
>
Node
>
Subnode

Audit of care of patients with congenital adrenal hyperplasia due to 21-Hydroxylase deficiency in a referral hospital in South India

Bhaskaran, S.; Nair, V.; Kumar, H.; Jayakumar, R.V.

Indian Pediatrics 43(5): 419-423

2006

ISSN/ISBN: 0019-6061
PMID: 16735765
Document Number: 599648
We carried out an audit of management of patients with 21-Hydroxylase deficiency CAH who presented to the Department of Endocrinology OPD from 1999 till 2004 and had a minimum follow up of 6 months. Of the 30 patients analysed 24 were girls and 6 were boys. The majority belonged to the Christian community. One third had a history of consanguinity or family history of similar illness. Sex assignment was appropriate in most. Karyotyping was done in half. Half the patients had adequate follow up and 17 OHP measurements. Only 7 out of 30 children had normal height for age. Bone age was done in 16 patients only. Most were on hydrocortisone. The average age of genital surgery was 31 months.

Document emailed within 1 workday
Secure & encrypted payments

Gutai, J.P.; Lee, P.A.; Johnsonbaugh, R.E.; Gareis, F.; Urban, M.D.; Migeon, C.J. 1979: Detection of the heterozygous state in siblings of patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency Journal of Pediatrics 94(5): 770-772
Dumić, M.; Brkljacić, L.; Krzisnik, C.; Radica, A.; Tajić, M.; Kastelan, A. 1983: Connection between congenital adrenal hyperplasia due to 21-hydroxylase deficiency and the HLA genotype Lijecnicki Vjesnik 105(7-8): 290-292
Vlaski, J.; Katanić, D.; Kavecan, I.; Dautović, S.; Vorgucin, I. 2008: Congenital adrenal hyperplasia due to 21 hydroxylase deficiency--case report Medicinski Pregled 61(3-4): 183-186
Adachi, R. 1991: Prenatal diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency with DNA analysis Nihon Sanka Fujinka Gakkai Zasshi 43(2): 227-233
Dumić, M.; Plavsić, V.; Brkljacić, L.; Sarnavka, V.; Mardesić, D.; Tajić, M.; Kastelan, A. 1983: Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency - different HLA genotypes in 2 brothers Lijecnicki Vjesnik 105(4): 145-149
Agboola-Abu, C.F.; Aligwekwe, P.K.; Olowu, A.O.; Kuku, S.F. 1999: Congenital adrenal hyperplasia due to 11-hydroxylase enzyme deficiency in three siblings. A brief report West African Journal of Medicine 18(2): 80-86
Schaison, G.; Gilbert-Dreyfus 1974: Late-appearing congenital adrenal hyperplasia. Apropos of 3 cases of 11 beta hydroxylase deficiency Annales de Medecine Interne 125(2): 163-168
Cattani, A.; Mahaha, D.; Michaud, P.; Rodríguez, J.A.; López, J.M.; García, H.; Foradori, A.; Velásquez, C.G. 1984: Virilizing congenital adrenal hyperplasia due to 21-hydroxylase deficiency: early diagnosis and response to 2 treatment schedules Revista Chilena de Pediatria 55(6): 374-379
Zacharías, S.; Contreras, P. 1984: Hirsutism secondary to congenital adrenal hyperplasia caused by a 21-hydroxylase deficiency of late onset. a clinical case Revista Chilena de Obstetricia y Ginecologia 49(5): 295-299
Bey-Omar, F.; Feit, J.P.; Forest, M.G.; David, M. 1983: Aggravation of salt loss due to hydrocortisone in the first days of treatment of congenital adrenal hyperplasia caused by 21-hydroxylase deficiency Pediatrie 38(2): 77-86
Turowska-Heydel, D. 1995: Classical form of congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Genetic considerations in light of personal studies Przeglad Lekarski 52(1): 10-12
Osinovskaia, N.S.; Ivashchenko, T.E.; Baranov, V.S. 2004: Analysis of the association of HLA-DQ1 alleles with mutation of the 21-hydroxylase gene in patients with congenital adrenal hyperplasia Genetika 40(1): 97-101
Hochberg, Z.; Even, L.; Zadik, Z. 1991: Mineralocorticoids in the mechanism of gynecomastia in adrenal hyperplasia caused by 11 beta-hydroxylase deficiency Journal of Pediatrics 118(2): 258-260
Bouchard, M.; Forest, M.G.; David, M.; Dechaud, H.; Juif, J.G. 1989: Familial congenital adrenal hyperplasia caused by 11 beta-hydroxylase. Failure of prevention of sexual ambiguity and prenatal diagnosis Pediatrie 44(8): 637-640
Pollack, M.S.; Maurer, D.; Levine, L.S.; New, M.I.; Pang, S.; Duchon, M.A.; Owens, R.P.; Merkatz, I.R.; Nitowsky, H.M.; Sachs, G.; Dupont, B. 1979: HLA typing of amniotic cells: the prenatal diagnosis of congenital adrenal hyperplasia (21-OH-deficiency type) Transplantation Proceedings 11(4): 1726-1728
Bhanji, R.; Khan, A.H.; Balouch, I.L.; Sabir, S.; Nazir, Z.; Billoo, A.G. 2004: Profile of children with congenital adrenal hyperplasia--a hospital study Jpma. Journal of the Pakistan Medical Association 54(10): 509-512
Boehm, B.O.; Rosak, C.; Boehm, T.L.; Kuehnl, P.; White, P.C.; Schöffling, K. 1986: Classical and late-onset forms of congenital adrenal hyperplasia caused by 21-OH deficiency reveal different alterations in the C4/21-OH gene region Molecular Biology and Medicine 3(5): 437-448
Dekker, L.; Houtzager, T.; Kilume, O.; Horogo, J.; van Roosmalen, J.; Nyamtema, A.Sadock. 2018: Caesarean section audit to improve quality of care in a rural referral hospital in Tanzania Bmc Pregnancy and Childbirth 18(1): 164
Wells, G.; Acton, R.T.; Azziz, R. 1993: Concordance of 21-hydroxylase gene ratio, human leukocyte antigen haplotyping and adrenal testing results in a family with late-onset adrenal hyperplasia Journal of Reproductive Medicine 38(8): 615-620
Jaruratanasirikul, S.; Thongseiratch, T. 2013: Diagnosis and management of congenital adrenal hyperplasia: 20-year experience in Songklanagarind Hospital Journal of the Medical Association of Thailand 96(3): 288-293