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Indian Pediatr ; 50(6): 605-7, 2013 Jun 08.
Article in English | MEDLINE | ID: mdl-23942406

ABSTRACT

We report Rhizomelic Chondrodysplasia Punctata (RDCP), a rare, autosomal recessive disorder with rhizomelic shortening of limbs, congenital cataracts and seizures but without any biochemical abnormality. The mother of the baby developed Systemic Lupus Erythromatosus (SLE) with Ro/SSA antibodies 11 months after delivery. Ro/SSA antibodies may generate calreticulin antibodies causing characteristic skeletal changes.


Subject(s)
Chondrodysplasia Punctata, Rhizomelic/diagnosis , Lupus Erythematosus, Systemic/diagnosis , Autoantibodies/analysis , Autoantigens/analysis , Chondrodysplasia Punctata, Rhizomelic/immunology , Humans , Infant, Newborn , Lupus Erythematosus, Systemic/immunology , Male , Mothers , RNA, Small Cytoplasmic/analysis , Ribonucleoproteins/analysis
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