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About 355 results

ALLMedicine™ Addison Disease Center

Research & Reviews  171 results

Death Due to Adrenal Crisis: Case Report and a Review of the Forensic Literature.
https://doi.org/10.1097/PAF.0000000000000678
The American Journal of Forensic Medicine and Pathology; Gitto L, Stoppacher R et. al.

Apr 9th, 2021 - Adrenal crisis is a life-threatening manifestation of acute adrenal insufficiency. One of the most important underlying causes is Addison disease (primary adrenal insufficiency).A 42-year-old White woman with a medical history of Addison disease o...

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...

Improved Urinary Cortisol Metabolome in Addison Disease: A Prospective Trial of Dual-Re...
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7947853
The Journal of Clinical Endocrinology and Metabolism; Espiard S, McQueen J et. al.

Nov 25th, 2020 - Oral once-daily dual-release hydrocortisone (DR-HC) replacement therapy has demonstrated an improved metabolic profile compared to conventional 3-times-daily (TID-HC) therapy among patients with primary adrenal insufficiency. This effect might be ...

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...

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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  179 results

Death Due to Adrenal Crisis: Case Report and a Review of the Forensic Literature.
https://doi.org/10.1097/PAF.0000000000000678
The American Journal of Forensic Medicine and Pathology; Gitto L, Stoppacher R et. al.

Apr 9th, 2021 - Adrenal crisis is a life-threatening manifestation of acute adrenal insufficiency. One of the most important underlying causes is Addison disease (primary adrenal insufficiency).A 42-year-old White woman with a medical history of Addison disease o...

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...

Improved Urinary Cortisol Metabolome in Addison Disease: A Prospective Trial of Dual-Re...
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7947853
The Journal of Clinical Endocrinology and Metabolism; Espiard S, McQueen J et. al.

Nov 25th, 2020 - Oral once-daily dual-release hydrocortisone (DR-HC) replacement therapy has demonstrated an improved metabolic profile compared to conventional 3-times-daily (TID-HC) therapy among patients with primary adrenal insufficiency. This effect might be ...

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...

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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 →