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Association of migraine-like headaches with Schimke immuno-osseous dysplasia

Authors :
Graham Smith
Jean Luc André
Anja Stein
Jorge M. Saraiva
Isabel Cordeiro
Nastasa Stajic
Cornelius F. Boerkoel
Leah I. Elizondo
Sara Sebnem Kilic
Thomas Lücke
Giuliana Lama
David V. Milford
Georges Deschênes
Doris Taha
Radovan Bogdanovic
Sandra Cockfield
Dorothea Wand
Dawna L. Armstrong
Ilkka Kaitila
Osman Dönmez
Beate Schmidt
Lydia Najera
Francisco Rodrigo
Petra Lamfers
Emily A. Sloan
Stefan Fründ
Cheng Huang
Uludağ Üniversitesi/Tıp Fakültesi/Çocuk Sağlığı ve Hastalıkları Anabilim Dalı.
Uludağ Üniversitesi/Tıp Fakültesi/İmmünoloji Anabilim Dalı.
Uludağ Üniversitesi/Tıp Fakültesi/Nefroloji Anabilim Dalı.
Kılıç, Sara Şebnem
Dönmez, Osman
AAH-1658-2021
Source :
American journal of medical genetics. Part A. 135(2)
Publication Year :
2005

Abstract

Schimke immuno-osseous dysplasia (SIOD) is characterized by spondyloepiphyseal. dysplasia, nephropathy, and T-cell deficiency. SIOD is caused by mutations in the putative chromatin remodeling protein SAL&RCAL1. We report an 8-year-old boy with SIOD and recurrent, severe, refractory migraine-like headaches. Through a retrospective questionnaire-based study, we found that refractory and severely disabling migraine-like headaches occur in nearly half of SIOD patients. We have also found that the vasodilator minoxidil provided symptomatic relief for one patient. We hypothesize that these headaches may arise from an intrinsic vascular, neuroimmune, or neurovascular defect resulting from loss of SMARCAL1 function.

Details

ISSN :
15524825
Volume :
135
Issue :
2
Database :
OpenAIRE
Journal :
American journal of medical genetics. Part A
Accession number :
edsair.doi.dedup.....70071d592885bfe37ee8e1ce930e8645