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Indian Pediatr. 2009 Jun;46(6):532-4.

Carbonic anhydrase II deficiency a novel mutation.

Author information

1
Department of Pediatric Genetics, Amrita Institute of Medical Sciences and Research Center, Aims Ponekkara, PO, Cochin, Kerala, India; and Metabolic Disease Unit, Safra Children Hospital, Sheba Medical Center, Tel Hashomer, Israel. sheelaknpn@yahoo.co.in

Abstract

Carbonic anhydrase II (CA II) deficiency is an extremely rare autosomal recessive disorder, characterised by a triad of osteopetrosis, renal tubular acidosis and cerebral calcifications. A 12 year old boy with classical features of CA II deficiency is reported who was found to be homozygous for the mutation in CA II gene and parents were heterozygous for the same mutation .To the best of our knowledge this is the first case report of mutation proven CA II deficiency from India.

PMID:
19556665
[Indexed for MEDLINE]
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