Bone marrow transplantation corrects osteopetrosis in the carbonic anhydrase II deficiency syndrome

C McMahon, A Will, P Hu, GN Shah… - Blood, The Journal …, 2001 - ashpublications.org
C McMahon, A Will, P Hu, GN Shah, WS Sly, OP Smith
Blood, The Journal of the American Society of Hematology, 2001ashpublications.org
Carbonic anhydrase II (CAII), found in renal tubules, brain, and osteoclasts, is critical in acid-
base homeostasis and bone remodeling. Deficiency of CAII gives rise to a syndrome of
osteopetrosis, renal tubular acidosis (RTA), and cerebral calcification with associated
developmental delay. It is inherited in an autosomal recessive fashion and found most
frequently in the Mediterranean region and the Middle East. We report 2 related Irish families
with clinically severe CAII deficiency in whom the gene mutation has been fully elucidated …
Abstract
Carbonic anhydrase II (CAII), found in renal tubules, brain, and osteoclasts, is critical in acid-base homeostasis and bone remodeling. Deficiency of CAII gives rise to a syndrome of osteopetrosis, renal tubular acidosis (RTA), and cerebral calcification with associated developmental delay. It is inherited in an autosomal recessive fashion and found most frequently in the Mediterranean region and the Middle East. We report 2 related Irish families with clinically severe CAII deficiency in whom the gene mutation has been fully elucidated. Two children, one from each family, have undergone allogeneic bone marrow transplantation because of severe progressive visual and hearing loss. The older 2 children had already developed cerebral calcification and marked visual loss at the time of diagnosis and were treated symptomatically. Post-transplantation evaluation at 2 and 3 years demonstrates histologic and radiologic resolution of their osteopetrosis with stabilization of hearing and vision. Both children remain developmentally delayed and continue to have RTA, and the older child has now developed cerebral calcification. Allogeneic bone marrow stem cell replacement cures the osteoclast component of CAII deficiency and retards the development of cerebral calcification, but it appears to have little or no effect on the renal lesions.
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