Search

everythinglearnresearchcommunity

for

Search:↓

Severe alopecia areata may increase the risk of hidden artery disease.

A man with a weakened immune system was diagnosed with a rare skin condition called trichodysplasia spinulosa using skin examination techniques.

A boy on a ketogenic diet and anti-epileptic drugs developed skin issues due to stopping vitamin supplements, which improved with proper supplementation.

The enzyme DHHC13 is essential for healthy hair and skin, and its deficiency leads to hair loss and skin problems.

Dysplastic nevi have unique gene expressions, making them distinct from common melanocytic nevi.

Younger patients with severe alopecia areata often have nail problems.

Three related Persian cats have a rare, likely hereditary skin condition causing hair loss and poor coat quality, with limited treatment options.

The girl had harmless hair casts, not lice.

Mice with the 'lanceolate hair' mutation have abnormal hair and skin similar to human Netherton's syndrome.

Skin symptoms can indicate endocrine disorders and have various treatments.

Switching insulin brands caused skin lesions in a diabetic woman, resolved by changing to oral medication.

Congenital atrichia with papular lesions causes permanent hair loss and skin bumps from birth.

Plica neuropathica can occur with diffuse alopecia and should be considered in diagnosis.

Isolated amylase deficiency can cause failure to thrive and should be checked with specific tests.

Malabsorption can cause skin issues like pigmentation changes and hair loss, which improve with treatment.

Thinner hair follicle structures are linked to non-scar alopecia.

Abnormal cuticle and hair shaft medulla cause hair loss in androgenetic alopecia; sonography helps diagnose and manage it.

A 17-year-old developed woolly hair nevus in adolescence, which is unusual, and over time the hair darkened and straightened slightly, but microscopic changes persisted.

The Shaven mutation in mice affects hair growth and causes a greasy coat due to abnormal lipid content.

Fresh plasma transfusions did not help treat Leiner disease in an infant.

The patient's long-term symptoms were due to Sheehan's syndrome, which improved with hormone therapy.

Biotin treatment improves symptoms of biotinidase deficiency, but some neurological damage may be permanent.

The case suggests that dissecting cellulitis of the scalp can occur in a White child and should be considered when diagnosing pediatric scarring alopecia.

A patient with Sézary syndrome showed improvement after treatment and the study suggested follicular mucinosis might indicate future lymphoma risk.

A new genetic variant causes BRESHECK syndrome by disrupting cell growth and stress response.

Skin changes and high vitamin B12 levels can be early signs of cancer.

Keratin is crucial for skin barrier formation and affects mitochondrial function.

Identical twins with a rare KRT 86 gene mutation both have the hair disorder monilethrix.

Pili torti hair is fragile due to loose keratin filaments and weak disulfide bonds.

A 15-year-old boy was correctly diagnosed with a rare skin condition after initially being misdiagnosed.