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Uncombable hair syndrome causes frizzy hair and can affect the nervous system, eyes, and ears, often co-occurring with other hair, skin, nail, and teeth conditions, and is linked to three specific gene mutations.

Rectangular black granules, solitary yellow dots, and mostly single-hair follicles suggest Loose Anagen Hair Syndrome.

Hair keratin-associated proteins are essential for strong hair, with over 80 genes showing specific patterns and variations among people.

A 5-year-old girl has sparse, dry, and brittle hair but is otherwise healthy.

Hair ages due to genetics and environmental factors, leading to graying and thinning, with treatments available for some conditions.

Advanced imaging techniques are crucial for accurately diagnosing Monilethrix, a rare hair disorder.

The study concluded that similar pathways regulate hair growth in dogs and mice, and these pathways are disrupted in dogs with Alopecia X, affecting stem cells and hormone metabolism.

PRP injections are not effective for long-term treatment of temporal triangular alopecia.

The document concludes that non-endocrine alopecia in pets varies in treatment effectiveness and often has a poor prognosis, especially in cats.

Trichoscopy is good for telling apart tinea capitis and alopecia areata in kids.

Some skin conditions are associated with other serious diseases, and office microscopy may miss many fungal infections.

Certain genetic variants are linked to frontal fibrosing alopecia in Spanish patients.

Dermoscopy is a good, noninvasive way to see normal cat skin structures and could be useful for check-ups.

Wnt/β-catenin signaling is important for keeping skin cell attachment structures stable.

A specific genetic change in the KRT71 gene causes a hair loss condition in Hereford cattle.

New treatments for immune disorders caused by FOXN1 deficiency are promising.

A woman's hair changed to a dry, tangled texture that's hard to comb after treatment with spironolactone, suggesting the medication might cause such hair changes.

Genetic testing is crucial for diagnosing congenital atrichia, a rare condition causing irreversible hair loss.

Fungal infection was the main cause of hair loss in Egyptian children studied.

A genetic mutation in the SGK3 gene causes hairlessness in Scottish Deerhounds and may relate to human hair loss.

Most hair loss in children is caused by a few common conditions and is easy to diagnose, but rare types require careful evaluation.

Mice with LSS deficiency showed hair loss and cataracts, similar to humans, and can help in understanding and treating this condition.

A young cat had a rare hair condition with twisted hair shafts but stayed healthy.

Obstetrician/gynecologists can diagnose and manage female hair loss with careful history taking and examination.

Five Weimaraners had a milder form of color dilution alopecia causing hair loss and skin issues.

Telogen Effluvium is a common hair loss condition that can be short-term or long-lasting and is often caused by stress, illness, or nutritional issues.

Accurate diagnosis and tailored treatments are crucial for managing hair loss in humans and animals.

A specific thyroid hormone resistance mutation may be linked to different types of hair loss.

Trichoscopy is a quick, accurate, and non-invasive method to diagnose and treat non-scarring hair loss.

The new treatment regimen was effective in promoting significant hair growth in all 15 male patients with androgenic alopecia.