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Liver damage in PCOS is linked to iron overload and cell death due to the miR-761-hepcidin/GPX4 pathway.

The man was diagnosed with Cronkhite-Canada syndrome, a rare disorder with GI polyps, skin issues, hair loss, and nail problems.

Enteral supplements can improve symptoms of Cronkhite-Canada syndrome.

Recognizing unusual symptoms in Crohn's disease is crucial for proper treatment.

A Japanese man with rare skin conditions improved with hydroxychloroquine treatment.

Two siblings with a rare type of rickets and hair loss had low vitamin D levels, which is not typical for their condition.

Localized hair growth and fat loss may share a common cause in lupus panniculitis.

Zinc deficiency in alcoholic cirrhosis patients causes skin issues, and zinc treatment improves symptoms.

A newborn with severe low blood sugar due to a genetic issue needed major surgery after standard treatments failed.

Different harmful mutations in the CDH3 gene cause HJMD, but symptoms vary among individuals.

RHUPUS should be considered in children with deforming arthritis.

Photodynamic therapy may not work for erythroplasia of Queyrat and could lead to invasive squamous cell carcinoma.

Infant baboons suffered from zinc poisoning due to poor cage conditions.

Selenium deficiency caused symptoms in a child, which improved with selenium supplements.

Some skin diseases and anaemia are related, and treating the skin condition can often improve the anaemia.

Oral Janus kinase inhibitors may be an effective treatment option for lichen planopilaris with some risk of increased cholesterol and liver enzyme levels.

Some men lost hair after deoxycholic acid treatment for neck fat, but most saw improvement or resolution.

Thyroid disease can cause skin and hair changes, treatable with levothyroxine.

A new genetic mutation was found causing hair and eye issues in a boy.

A baby with a rare metabolic disorder developed a rash not cured by zinc alone, likely due to both zinc and amino acid deficiencies.

21-hydroxylase deficiency causes hormone imbalances leading to various symptoms, and diagnosis involves clinical and genetic tests.

A young woman's Cronkhite-Canada syndrome improved on its own after she gave birth.

The research linked PLCD1 gene variants to the development of trichilemmal cysts.

Lead and selenium levels don't cause premature graying.

A 13-year-old boy had both lichen planus and vitiligo, suggesting a possible link between the two conditions.

Two sisters had rare, widespread cysts and complete hair loss, suggesting a genetic link.

Chronic cutaneous lupus erythematosus causes scarring, hair loss, and skin discoloration, especially on sun-exposed areas.

A rare skin condition causes red and dark patches on the face and limbs.

Women with PCOS and higher androgen levels are more likely to have fatty liver disease.

Accurate diagnosis of APL is crucial to avoid unnecessary treatments.