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AGA might indicate higher risk for severe COVID-19.

A new ARID1B gene variation causes Coffin-Siris syndrome 1 and early high myopia in a Chinese family.

The patient with lupus and Degos' disease showed significant improvement with treatment.

A 3-year-old with vitamin D-resistant rickets and severe hair loss died despite treatment, highlighting the need for improved management of the condition.

A woman with a rare hormone resistance condition also had missing teeth and hair loss, which might be new symptoms of her genetic disorder.

Topical tofacitinib helped a man with severe scalp condition after other treatments failed.

The document discusses various eye conditions and their treatments, including a rare eye cancer in a baby, vision loss from a cancer drug, cataracts from a baldness treatment, a rare skin disorder, and a specific type of eye disease diagnosed with a special imaging technique.

The girl in "The Girl with a Pearl Earring" might have had alopecia areata, causing her lack of eyebrows and sparse eyelashes.

Aire mutation reduces alopecia areata, while Notch4 mutation prevents it in mice.

Farudodstat may effectively treat alopecia areata by protecting hair follicles without harmful effects.

The gene HDC is important for the development of hair follicles in newborn mice.

Fluocinolone may help treat scalp symptoms in ichthyosis patients.

A rare skin condition caused scarring hair loss on the scalp.

3D-ultrasound can non-invasively detect and predict alopecia areata phases and outcomes.

Finasteride causes reduced tear flow and severe eye inflammation.

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

WWP2 is crucial for tooth development in mice.

A child with ectodermal dysplasia-syndactyly syndrome has a new mutation in the NECTIN4 gene.

Sympathetic activation and venous tone are crucial for heart failure symptoms.

A post-COVID-19 patient in Manaus developed cryptococcal meningitis, highlighting the need for better health education and sanitation.

Mechanoreceptors convert physical touch into electrical signals through specialized nerve structures.

Trichoscopy can diagnose Netherton syndrome without pulling hairs.

Removing part of the vitamin D receptor stops vitamin D from working properly.

Squaric acid dibutylester for alopecia areata can cause benign skin lymphoid growths.

A new genetic mutation in the hairless gene causes a rare hair loss disorder.

Certain cells in the adult mouse ear come from cranial neural crest cells, but muscle and hair cells do not.

FOXN1 mutations cause severe immunodeficiency, hair loss, nail issues, and thymus defects.

Folliculitis decalvans mainly affects middle-aged African American men and is treated with antibiotics.

Tofacitinib may effectively treat folliculitis decalvans.