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Rhizomelic Chondrodysplasia Punctata
This cutaneous condition: known as Rhizomelic Chondrodysplasia Punctata, can be Discussed here.
Persons finding themselves or loved ones distressed in their lives because of Rhizomelic chondrodysplasia punctata (Autosomal recessive chondrodysplasia punctata type 1, Chondrodystrophia calcificans punctata, Peroxisomal biogenesis disorder complementation group 11) may like to share how they cope in order to help others world-wide searching for experiences.
Girl With Rare and Deadly Dwarfism Given One Year to Live. But She Defies the Odds
In Australia, Isabela Corstorphan was born with an extremely rare form of dwarfism called Rhizomelic Chondrodysplasia Punctata (RCDP). According to the United States National Library of Medicine, the condition is characterized by a shortening of bones in the upper arms and thighs. However, the condition also causes intellectual disability, skeletal abnormalities, respiratory problems, heart issues, seizures and many other physical problems. Ref. Source 6r