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Trichoscopy is a useful tool for diagnosing and managing hair and scalp conditions, often better than traditional methods.

Most adrenal cortex tumors are benign and non-secreting, but proper diagnosis and treatment are important due to the rare possibility of cancer.

Acne is a common skin condition linked to diet, hormones, and genetics, and early treatment can prevent scarring.

Drug metabolism affects how long a drug works, its interactions, activation, and toxicity, and is influenced by genetics, diet, illness, and other drugs.

Certain genetic variants linked to immune response increase the risk of alopecia areata in Taiwanese people.

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

Low-coverage sequencing is a cost-effective way to identify genes related to wool traits in rabbits.

A 12-year-old boy with twenty nail dystrophy, a condition affecting all nails, was treated conservatively due to its self-limiting nature and good prognosis.

A new mutation in the TMEM173 gene and a risk allele in IFIH1 cause a unique set of immune-related symptoms.

Hidradenitis suppurativa is a chronic skin condition more common in women, linked to genetics and lifestyle factors, and associated with various other health issues.

A 19-year-old male had two rare skin conditions causing scarring and permanent hair loss.

Melanocytes produce melanin; their defects cause vitiligo and hair graying, with treatments available for vitiligo.

Alopecia areata causes hair loss with varied treatment responses and frequent relapses.

Different types of inactive melanocyte stem cells exist with unique characteristics and potential to develop into other cells.

People with alopecia have a higher risk of thyroid cancer.

A specific genetic deletion in goats affects cashmere yield and thickness.

The 3D-SeboSkin model effectively simulates Hidradenitis suppurativa and is useful for future research.

Dermal Papilla Cells grown in 3D and with stem cells better mimic natural hair growth conditions than cells grown in 2D.

The document explains various skin conditions and their treatments.

Skin symptoms can indicate endocrine disorders and have various treatments.

The document concludes that accurate diagnosis and treatment are crucial in dermatology, and it presents various findings on skin conditions and treatments.

Keratin proteins are crucial for hair structure and strength.

People with Birt-Hogg-Dubé syndrome often have lung problems and delayed diagnosis, and better recognition of CT scan signs could improve diagnosis and management.

Early diagnosis of Trichorhinophalangeal syndrome type 1 is crucial for treatment and was achieved through clinical examination and family history.

A woman with a unique syndrome similar to TRPS has a genetic change near the TRPS1 gene, affecting its regulation.

The document concludes that while white skin, nail, and mucosa diseases increase skin cancer risk, they are generally harmless, especially compared to darker pigmentation conditions.

The protein FLCN is involved in cellular cleanup and is regulated by ULK1.

A TP63 gene mutation causes significant hair loss and mild skin, nail, and tooth abnormalities.

Long-term use of androgens can help manage Hereditary Angioedema (HAE) but may cause serious side effects, so alternative treatments with fewer side effects are being considered.

A girl with a rare skin condition called Keratosis Follicularis Spinulosa Decalvans showed no significant improvement with treatment.