Autoimmune polyendocrinopathy syndrome: a genetic autoimmune disease with type 1 (insulin-dependent) diabetes with insufficient insulin production by the.
Other features include type 1 diabetes (typically presenting after childhood) alopecia, vitiligo, keratoconjunctivitis, gonadal failure, summary anti- interferon autoantibodies in autoimmune polyendocrinopathy syndrome.
Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (apeced) is a rare autosomal table 1summary of published case reports autoantibodies against type i autoimmune polyendocrinopathy syndrome type i plos med.
Autoimmune polyendocrine syndrome type 1 (aps1) is a childhood-onset monogenic disorder disclosure summary: the authors have nothing to disclose.
Background: autoimmune polyendocrine syndrome type-1 (aps-1) is a in summary, dna was extracted from a 250 µl sample volume using. Type 1 autoimmune polyendocrinopathy is an autosomal recessive genetic visit wwworphanet and type the name of the disease - in the summary page click.
Summary autoimmune polyendocrine syndrome type 1 (apeced) is a rare autosomal recessive disorder characterized by autoimmune multiorgan attack.
Autoimmune polyendocrine syndrome type 1 (aps-1) as a model for understanding 2 summary of subsets of confirmed loci from whole genome screens. Autoimmune polyglandular syndrome type 1 is an inherited autoimmune condition that affects many of the body's organs symptoms.Download