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Too much vitamin A can cause liver damage and skin issues.

A small number of premenopausal female blood donors had high prolactin levels, often due to stress, and retesting is recommended to prevent misdiagnosis.

Graham-Little Piccardi Lassueur Syndrome is a rare skin condition with specific hair loss and skin symptoms.

Women in Australia report different signs of facial aging compared to women in the US, UK, and Canada; men with Lichen planopilaris often have hormonal abnormalities and thyroid disease.

Early recognition and aggressive treatment can significantly improve rare ANA-negative lupus with heart and skin issues.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

LIPH mutations cause woolly hair in some Chinese people.

Children with classic congenital adrenal hyperplasia have thicker heart fat and more heart and blood vessel risk factors, especially if their condition is not well-controlled.

A rare genetic mutation causes resistance to vitamin D, leading to severe rickets and requires high doses of calcium and vitamin D for management.

Rothmund-Thomson syndrome causes skin changes, hair loss, and slightly high lysine and cystine in urine.

Li2CO3 improved skin disease in a mouse model of Focal Dermal Hypoplasia without toxicity.

GLPLS is a rare skin condition with specific hair loss and skin symptoms.

Idiopathic hypoparathyroidism is rare and can be managed with dihydrotachysterol.

Low IGF-1 and high HDL cholesterol levels are linked to more hair loss in middle-aged women.

Mice lacking the PPARγ gene in their fat cells had almost no fat tissue, severe metabolic problems, and abnormal development of other fat-related tissues.

Rare ovarian tumors can cause increased male hormones in postmenopausal women; surgery is an effective treatment.

The man had pretibial myxedema and hyperthyroidism, causing skin changes and thyroid issues.

Ovarian stromal hyperplasia can cause high testosterone in postmenopausal women and is treated by removing the ovaries.

Autoimmune-related phenomena do not affect the progression or characteristics of lichen sclerosus in women.

Certain ESR1 gene variations may affect hormone levels and fat distribution in women with high male hormone levels.

Chronic cutaneous lupus erythematosus should be considered when acne treatments don't work.

PCOS women have more severe metabolic issues and higher androgen levels than hyperandrogenic women without PCOS.

A man with kidney tumors and lung cysts was diagnosed with Birt–Hogg–Dubé syndrome and treated successfully, with genetic testing confirming the diagnosis.

CD4+ lymphocytopenia can occur in patients with systemic lupus erythematosus.

Cholesterol and phospholipids increase in mouse skin during cancer development, with differences between male and female skin.

Two brothers from Bangladesh were diagnosed with X-linked adrenoleukodystrophy, showing neurological and adrenal symptoms.

Progeria causes early aging due to a gene mutation, affecting skin, bones, and heart, with treatments aimed at improving life quality.

A boy with a rare skin condition and kidney disease improved with cyclosporine after steroids failed, suggesting a new treatment approach.

The research found different metabolism changes in PCOS patients and suggested new potential markers for diagnosing PCOS with or without insulin resistance.

Oral lichen planus is not linked to sex hormone levels.