Abstract
A child with neonatal onset multi-systemic inflammatory disease (NOMID)
Highlights
Neonatal onset multi-systemic inflammatory disease (NOMID) is known as chronic, infantile, neurological, cutaneous, and articular (CINCA) syndrome and only around 100 cases have been identified worldwide[1]
Recurrent febrile episodes were present up to 2 years since infancy. He was noted to have poor head control until 7 months of age. He had global developmental delay which was accompanied by intellectual impairment
NOMID was first described by Prieur and Griscelli[2]
Summary
Neonatal onset multi-systemic inflammatory disease (NOMID) is known as chronic, infantile, neurological, cutaneous, and articular (CINCA) syndrome and only around 100 cases have been identified worldwide[1]. Case report A nine year old boy, second live born child to healthy, non-consanguineous parents with a healthy sibling, presented for further evaluation of short stature, global developmental delay and anaemia. He had recurrent urticaria from 4 months of age up to 9 years. He had global developmental delay which was accompanied by intellectual impairment.
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