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Alopecia areata causes varying hair loss patterns, affecting hair, nails, and possibly glands, with treatment outcomes depending on disease duration and extent.

The document concludes that careful diagnosis is crucial for chromosome 13q deletion syndrome, tamoxifen can cause reversible eye damage, finasteride may be linked to cataracts, and OCT is useful for diagnosing macular diseases.

A 2-year-old boy had no hair and unusual organ placement, and it's unclear if it's genetic or coincidental.

Most orthodontic patients with missing teeth also have hair disorders.

The skin is vital for protection, temperature control, fluid balance, immunity, and sensing, with damage affecting daily life and mental health.

Keratin-associated proteins have ancient origins and were used for different purposes before being adapted for hair in mammals.

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.

Recombinant thrombomodulin can effectively treat severe complications in Cronkhite-Canada syndrome.

Red and infrared light therapy improves hair growth in balding patients.

A 73-year-old man's grey-white hair turned dark brown after eczema treatment.

Lactic acid cream can help improve skin bumps known as eruptive vellus hair cysts.

Hair, teeth, and mammary glands develop similarly at first but use different genes later.

Hair loss from Telogen Effluvium usually gets better within 6 months after addressing the cause.

Genetic screening is crucial for accurately diagnosing APS-1 due to its varied symptoms.

A new PAX9 gene mutation causes missing teeth and hair problems, but not skin or nail issues.

Rabbits lacking the Hoxc13 gene show similar hair and skin issues to humans with ECTD-9, making them good for research on this condition.

A peptide called DPS-1 helps human scalp cells grow and stimulates hair growth in mice.

A patient with Cronkhite-Canada Syndrome developed colon cancer that spread to the liver, showing the need for regular cancer checks in such patients.

Congenital atrichia is a rare condition where children are born without hair, and treatment is often ineffective.

mTORC1 activity is important for hair growth and color, and targeting it could help treat hair loss and greying.

The ingredients could help prevent hair loss by promoting hair growth and increasing VEGF secretion.

Children's hair loss can be caused by various factors and should be treated with appropriate, age-specific methods and psychological support.

The anti-hair loss shampoo effectively promotes hair growth and improves hair quality.

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

Bovines can have rare inherited skin diseases with specific symptoms like hair loss, fragile skin, and abnormal porphyrin buildup.

A new medical syndrome may include skin changes, hair loss, sweating issues, bone malformations, leg swelling, and low cortisol.

Wnt/beta-catenin signaling in the skin helps fat cell development during hair growth and repair.

About 30% of women feel they lose too much hair, often starting before age 40, and most can't find a reason for it.

The document concludes that permanent hair loss conditions are complex, require early specific treatments, and "secondary permanent alopecias" might be a more accurate term than "secondary cicatricial alopecia."

Vitiligo is a skin condition causing white spots, more common in women, often starts before age 20, and can affect mental health.