Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Prakash S. Matadh"'
Publikováno v:
Indian journal of pediatrics. 72(4)
Fibrochondrogenesis is a rare lethal short-limb skeletal dysplasia. Till now only fifteen cases have been reported since Lazzaroni-Fossati first described it in 1978. Hence reported a case of fibrochondrogenesis in a child born to a consanguineously
Publikováno v:
The Indian Journal of Pediatrics. 74:787-789
Wharton's jelly is a specialized tissue which acts as supportive and protective structure substituting for the adventitia of the umbilical vessels. Absence of Wharton's jelly around the umbilical arteries is very rare and an unusual cause of perinata
Publikováno v:
Indian journal of pediatrics. 72(4)
Fibrochondrogenesis is a rare lethal short-limb skeletal dysplasia. Till now only fifteen cases have been reported since Lazzaroni-Fossati first described it in 1978. Hence reported a case of fibrochondrogenesis in a child born to a consanguineously
Autor:
M L, Kulkarni, Prakash S, Matadh
Publikováno v:
Indian pediatrics. 40(6)
Osteopetrosis is a hereditary bone disease with intense positive balance of body calcium. Infantile variety is often associated with rickets--a paradoxical association. Two siblings with osteopetro rickets are reported in the article. The pathophysio