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Autoimmune disorders in Kabuki syndrome.
- Source :
-
American journal of medical genetics. Part A [Am J Med Genet A] 2005 Jan 30; Vol. 132A (3), pp. 260-2. - Publication Year :
- 2005
-
Abstract
- Kabuki syndrome is associated with abnormalities in multiple organ systems. While many of the anomalies are congenital malformations, other clinical manifestations may not appear until later in childhood. Among these associated conditions, autoimmune abnormalities have been described in several patients. These include idiopathic thrombocytopenic purpura (ITP), hemolytic anemia, thyroiditis, and vitiligo. In this report, we describe five affected patients with autoimmune manifestations. Four patients had ITP, and two of these patients had concurrent hemolytic anemia. The fifth patient had vitiligo. Two of the patients with ITP had a chronic and relapsing course. Of note, some of these patients also had hypogammaglobulinemia. The autoimmune disorders may be manifestations of abnormal immune regulation. We conclude that Kabuki syndrome is associated with an increased incidence of autoimmune disorders. In addition, the presence of an underlying immune defect may predispose these children to a chronic course of these autoimmune conditions.<br /> ((c) 2004 Wiley-Liss, Inc.)
- Subjects :
- Abnormalities, Multiple genetics
Abnormalities, Multiple pathology
Adolescent
Autoimmune Diseases immunology
Child
Child, Preschool
Cleft Palate pathology
Female
Growth Disorders pathology
Humans
Intellectual Disability pathology
Karyotyping
Male
Purpura, Thrombocytopenic, Idiopathic immunology
Purpura, Thrombocytopenic, Idiopathic pathology
Syndrome
Vitiligo immunology
Vitiligo pathology
Abnormalities, Multiple immunology
Autoimmune Diseases pathology
Craniofacial Abnormalities pathology
Developmental Disabilities pathology
Subjects
Details
- Language :
- English
- ISSN :
- 1552-4825
- Volume :
- 132A
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- American journal of medical genetics. Part A
- Publication Type :
- Academic Journal
- Accession number :
- 15523604
- Full Text :
- https://doi.org/10.1002/ajmg.a.30332