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Familial autoinflammatory Behçet-like syndrome: A rare cause of failure to thrive in children
Payal Mittal1, Shuchi Bhalla2, Kapil Bhalla3
1Junior Resident, Department of Paediatrics, Pt. B.D. Sharma, PGIMS, Rohtak, Haryana, India.
Abstract:
Familial auto-inflammatory Behçet-like syndrome-1 is a rarely reported entity. The clinical manifestations of this condition mimic Behçet's disease in the form of recurrent oral ulcers and gastro-intestinal manifestations. The complete clinical spectrum is yet to be ascertained, as this is a genetic syndrome involving multiple mutations. Here, we report the case of a child with severe malnutrition and failure to thrive in infancy, who turned out to have the said genetic syndrome.
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