Schimke immuno-osseous dysplasia: A clinicopathological correlation

J. Marietta Clewing, Barbara C. Antalfy, Thomas Lücke, Behzad Najafian, Katja M. Marwedel, Akira Hori, Ralph M. Powel, A. F.Safo Do, Lydia Najera, Karen SantaCruz, M. John Hicks, Dawna L. Armstrong, Cornelius F. Boerkoel

Research output: Contribution to journalArticlepeer-review

41 Scopus citations

Abstract

Background: Schimke immune-osseous dysplasia (SIOD) is a fatal autosomal recessive disorder caused by loss-of-function mutations in swi/snf-related matrix-associated actin-dependent regulator of chromatin, subfamily α-like I (SMARCAL1). Methods: Analysis of detailed autopsies to correlate clinical and pathological findings in two men severely affected with SIOD. Results: As predicted by the clinical course, T cell deficiency in peripheral lymphoid organs, defective chondrogenesis, focal segmental glomerulosclerosis, cerebral ischaemic lesions and premature atherosclerosis were identified. Clinically unexpected findings included a paucity of B cells in the peripheral lymphoid organs, emperipolesis-like (penetration of one cell by another) abnormalities in the adenohypophysis, fatty infiltration of the cardiac right ventricular wall, pulmonary emphysema, testicular hypoplasia with atrophy and azospermia, and clustering of small cerebral vessels. Conclusions: A regulatory role for the SMARCAL1 protein in the proliferation of chondrocytes, lymphocytes and spermatozoa, as well as in the development or maintenance of cardiomyocytes and in vascular homoeostasis, is suggested. Additional clinical management guidelines are recommended as this study has shown that patients with SIOD may be at risk of pulmonary hypertension, combined immunodeficiency, subcortical ischaemic dementia and cardiac dysfunction.

Original languageEnglish (US)
Pages (from-to)122-130
Number of pages9
JournalJournal of medical genetics
Volume44
Issue number2
DOIs
StatePublished - Feb 2007

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