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A novel case of congenital fetal heart block in a mother with Addison's disease
Author(s) -
Orefice Roberto,
Paoletti Debra,
Robertson Meiri
Publication year - 2018
Publication title -
sonography
Language(s) - English
Resource type - Journals
eISSN - 2054-6750
pISSN - 2202-8323
DOI - 10.1002/sono.12154
Subject(s) - unit (ring theory) , medicine , fetal heart , general hospital , fetus , pediatrics , pregnancy , psychology , biology , genetics , mathematics education
Addison’s disease or primary adrenocortical insufficiency is a rare endocrine disorder. In the majority of cases, pathogenesis lies in idiopathic autoimmune adrenalitis, and 21-hydroxylase autoantibodies have been found in 80–90% of patients with idiopathic Addison’s disease. Addison’s disease can have a varied presentation from non-specific symptoms of weakness, fatigue, nausea and abdominal pain to classic skin pigmentation and hypotensive shock associated with an Addisonian crisis. This case demonstrates the first documented case of a woman with Addison’s disease with antenatally diagnosed complete fetal heart block. This may help to guide the management of future cases of fetal heart block with Addison’s and other autoimmune conditions.