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About 347 results

ALLMedicine™ Addison Disease Center

Research & Reviews  167 results

A Patient With AIRE Mutation Who Presented With Severe Diarrhea and Lung Abscess.
https://doi.org/10.1097/INF.0000000000002887
The Pediatric Infectious Disease Journal; Soyak Aytekin E, Serin O et. al.

Dec 7th, 2020 - Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED) (polyglandular endocrinopathy type 1) is a rare autosomal recessive disorder caused by mutations in the autoimmune regulator gene (AIRE). The major clinical features of APECED...

A Case of Critical Lower-Limb Ischemia in a 29-Year-Old Man with Autoimmune Polyglandul...
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7579748
The American Journal of Case Reports; Ennab RM, Saadeh NA

Oct 17th, 2020 - BACKGROUND Autoimmune polyglandular syndrome type 1 (APS-1) is an extremely rare autoimmune disorder with an autosomal recessive inheritance pattern. Its manifestations present in chronological sequence of the components mucocutaneous candidiasis,...

Current Management and Outcome of Pregnancies in Women With Adrenal Insufficiency: Expe...
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7320831
The Journal of Clinical Endocrinology and Metabolism; Bothou C, Anand G et. al.

May 19th, 2020 - Appropriate management of adrenal insufficiency (AI) in pregnancy can be challenging due to the rarity of the disease and lack of evidence-based recommendations to guide glucocorticoid and mineralocorticoid dosage adjustment. Multicenter survey on...

Residual Corticosteroid Production in Autoimmune Addison Disease.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7274491
The Journal of Clinical Endocrinology and Metabolism; Sævik ÅB, Åkerman AK et. al.

May 11th, 2020 - Contrary to current dogma, growing evidence suggests that some patients with autoimmune Addison disease (AAD) produce corticosteroids even years after diagnosis. To determine frequencies and clinical features of residual corticosteroid production ...

Natural History of Adrenal Steroidogenesis in Autoimmune Addison's Disease Following Di...
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7250207
The Journal of Clinical Endocrinology and Metabolism; Napier C, Allinson K et. al.

Apr 17th, 2020 - The natural history of adrenal function in autoimmune Addison disease once diagnosed and treated has not been systematically studied, but several case reports of recovery from established adrenal failure suggest it may not be uniform. To ascertain...

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Guidelines  1 results

Consensus statement on the diagnosis, treatment and follow-up of patients with primary adren...
https://onlinelibrary.wiley.com/doi/abs/10.1111/joim.12162
Husebye, E.

Jan 31st, 2014 - Primary adrenal insufficiency (PAI), or Addison's disease, is a rare, potentially deadly, but treatable disease. Most cases of PAI are caused by autoimmune destruction of the adrenal cortex.

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Clinicaltrials.gov  175 results

A Patient With AIRE Mutation Who Presented With Severe Diarrhea and Lung Abscess.
https://doi.org/10.1097/INF.0000000000002887
The Pediatric Infectious Disease Journal; Soyak Aytekin E, Serin O et. al.

Dec 7th, 2020 - Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED) (polyglandular endocrinopathy type 1) is a rare autosomal recessive disorder caused by mutations in the autoimmune regulator gene (AIRE). The major clinical features of APECED...

A Case of Critical Lower-Limb Ischemia in a 29-Year-Old Man with Autoimmune Polyglandul...
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7579748
The American Journal of Case Reports; Ennab RM, Saadeh NA

Oct 17th, 2020 - BACKGROUND Autoimmune polyglandular syndrome type 1 (APS-1) is an extremely rare autoimmune disorder with an autosomal recessive inheritance pattern. Its manifestations present in chronological sequence of the components mucocutaneous candidiasis,...

Current Management and Outcome of Pregnancies in Women With Adrenal Insufficiency: Expe...
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7320831
The Journal of Clinical Endocrinology and Metabolism; Bothou C, Anand G et. al.

May 19th, 2020 - Appropriate management of adrenal insufficiency (AI) in pregnancy can be challenging due to the rarity of the disease and lack of evidence-based recommendations to guide glucocorticoid and mineralocorticoid dosage adjustment. Multicenter survey on...

Residual Corticosteroid Production in Autoimmune Addison Disease.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7274491
The Journal of Clinical Endocrinology and Metabolism; Sævik ÅB, Åkerman AK et. al.

May 11th, 2020 - Contrary to current dogma, growing evidence suggests that some patients with autoimmune Addison disease (AAD) produce corticosteroids even years after diagnosis. To determine frequencies and clinical features of residual corticosteroid production ...

Natural History of Adrenal Steroidogenesis in Autoimmune Addison's Disease Following Di...
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7250207
The Journal of Clinical Endocrinology and Metabolism; Napier C, Allinson K et. al.

Apr 17th, 2020 - The natural history of adrenal function in autoimmune Addison disease once diagnosed and treated has not been systematically studied, but several case reports of recovery from established adrenal failure suggest it may not be uniform. To ascertain...

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News  3 results

Vomiting, Weakness, and Skin Discoloration in a 9-Year-Old Child
https://www.medscape.com/viewarticle/726070_3

Aug 3rd, 2010 - Discussion Addison disease is a disorder of the adrenal glands that results in decreased production of steroids. It was first described by British physician Thomas Addison in 1855. The incidence of Addison disease is 40-60 cases per million, and t...

Vomiting, Weakness, and Skin Discoloration in a 9-Year-Old Child
https://www.medscape.com/viewarticle/726070_2

Aug 3rd, 2010 - Case Summary This patient's presentation to the ED can be concisely summarized to contribute to the diagnosis of Addison disease with adrenal crisis: weakness, vomiting, abdominal pain, abnormal skin and mucous membrane coloring, hypotension, tach...

Addisonian Pigmentation of the Oral Mucosa
https://www.mdedge.com/dermatology/article/67263/addisonian-pigmentation-oral-mucosa
Shah SS, Oh CH et. al.

Cutaneous pigmentation is a hallmark of Addison disease. When present, the hyperpigmentation generally localizes to sun-exposed surfaces.

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Patient Education  1 results see all →