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J Pediatr. 2000 May;136(5):682-7.

Response to steroid therapy in autism secondary to autoimmune lymphoproliferative syndrome.

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1
Divisions of Hematology-Oncology, Neurology, and Immunology-Rheumatology, Department of Pediatrics, Washington University School of Medicine and St Louis Children's Hospital, St Louis, MO 63110, USA.

Abstract

We report a child who developed autoimmune lymphoproliferative syndrome (ALPS) secondary to a heterozygous dominant negative mutation in the death domain of the Fas receptor. Previously developmentally normal, he had symptoms of autism with rapid regression in developmental milestones coincident with the onset of lymphoproliferation and autoimmune hemolytic anemia. Low-dose steroid therapy induced early and complete remission in the ALPS phenotype. There was subjective improvement, followed by objective improvement in speech and developmental milestones. We propose that autism may be part of the autoimmune disease spectrum of ALPS in this child, and this case represents a novel manifestation and target organ involvement in this disease.

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PMID:
10802504
DOI:
10.1067/mpd.2000.105355
[Indexed for MEDLINE]
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