Abstract
Three cases of Conradi disease are presented to highlight the distinct clinical features and to emphasize the differentiation of the two types.
Similar content being viewed by others
References
Comings DE, Papazian C, Schoene HR: Conradi’s disease. J Pediatr 72: 63, 1968
Spranger JW, Bidder U, Voelz C: Chondrodystrophia punctata-Type Conradi Hunnerman-Foetschr-Roentengenstr. 113: 717, 1970
Bhushan V, Anand NK, Shah MM, Saini L: Chondrodystrophia calcificans punctata. Indian Pediatr 13:261, 1978
Singh V, Lal H, Singh N, Ramkumar L: Conradi’s disease (chondrodystrophia calcificance congenita). Indian Pediatr 15: 1043, 1978
Yakovac WC: Calcirous chondropathies in the newborn infant. Arch Path 57:62, 1959
Becker MH, Genieser NB, Finegold M, Miranda D, Spackman T: Chondrodysplasia punctata (Is maternal Warfarin therapy a factor ?)-Am J Dis child 129:356, 1976
Patton RG, Christie DL, Smith DW, Beckwith JB: Cerebrohepatorenal) syndrome of Zellweger. Am J Dis Child 124: 840, 1972
Hyndmann WB, Alexander DS, Mackie KW: Chondrodystrophic calcificans congenita (The Conradi-Hunnermann Syndrome). Clinical Paediatrics 15:317, 1976
Smith DW, Syndrome Lemli L, Opitz JM: A new recognised of multiple congenital anomalies. J Pediatr 64: 210, 1964
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
Merchant, R.H., Shah, K.N., Mehta, K.P. et al. Diagnosis and counselling in Conradi disease. Indian J Pediatr 49, 767–769 (1982). https://doi.org/10.1007/BF02752666
Issue Date:
DOI: https://doi.org/10.1007/BF02752666