-
Achondroplasia is a
genetic disorder with an
autosomal dominant pattern of
inheritance whose primary feature is dwarfism. It is the most
common cause of...
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Rhizomelic chondrodysplasia punctata is a rare
developmental brain disorder characterized by
abnormally short arms and legs (rhizomelia), seizures, recurrent...
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chondrodysplasia punctata (autosomal
recessive chondrodysplasia punctata type 1,
chondrodystrophia calcificans punctata,
peroxisomal biogenesis disorder complementation...
- Short-Limbed Dwarf, With
Special Reference To
Osteogenesis Imperfecta and
Chondrodystrophia Foetalis". The
American Journal of the
Medical Sciences. 125 (5)....
- Sep., 1963 2. Paul SS, Rao PL,
Mullick P,
Kalliana P "A Case of
Chondrodystrophia Calcificans Congenita". Arch Dis
Child 1963 38: 632-635. doi: 10.1136/adc...
- 58 (1): 22–23. PMC 5178695. PMID 29007957. Das, K (1909). "Foetal
Chondrodystrophia as a
Cause of Brow
Presentation and Dystocia". Proc. R. Soc. Med....
