Search

everythinglearnresearchcommunity

for

Search:↓

The report concludes that atypical Brauer nevus is more common in males, present at birth, and often misdiagnosed due to its unusual scalp locations.

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

Minoxidil stimulates hair growth by increasing hair thickness and prolonging growth phase.

Some horses lose hair without inflammation or itching due to various conditions, and while mainly a cosmetic issue, diagnosis requires examination and biopsies, and breeding is not advised if it's hereditary.

Understanding normal hair growth and loss in children is key to diagnosing and treating hair disorders.

Minoxidil promotes hair regrowth, but more research needed for effectiveness and response factors.

The absence of functional sebaceous glands causes hair follicle destruction and scarring alopecia.

AIRE protein, defective in APECED patients, is found in skin and hair cells and interacts with cytokeratin 17.

sPLA2-X is crucial for normal hair growth and follicle health.

Knocking out certain genes in mice helps understand skin and hair growth problems.

KFSD is a genetic disorder causing hair loss and skin issues, with no effective treatment.

Hair follicle bulge cells don't help skin regrow after glucocorticoid damage; interfollicular epidermis cells do.

β-catenin in the dermal papilla is crucial for normal hair growth and repair.

Blocking Wnt signaling in young mice causes thymus shrinkage and cell loss, but recovery is possible when the block is removed.

Minoxidil helps grow longer, thicker hair in bald scalps of stumptailed macaques, and early treatment is more effective.

Testosterone and dihydrotestosterone affect hair growth, and new techniques like the folliculogram help study it, but fully understanding hair growth is still complex.

Losing eyelashes or eyebrows can be a sign of many different health problems and needs a careful approach to treat effectively.

People with X-linked hypohidrotic ectodermal dysplasia have no sweat ducts and less, thinner hair.

Alternative treatments show promise for hair growth beyond traditional methods.

Hair color is influenced by genetics and can indicate certain health conditions.

The document describes a rare case of IFAP syndrome, a genetic condition with symptoms of hair loss, light sensitivity, and scaly skin.

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

Hair transplantation effectively treated a bald patch in an 18-year-old woman with Temporal Triangular Alopecia.

Vitamin D receptor is crucial for starting hair growth after birth.

Shaving caused a mild, itchy pubic rash with small bumps and crusts.

Sox21 is crucial for tooth development and enamel formation by preventing cells from changing into a different type.

New gene variants linked to a rare inherited hair loss disorder were found in three Chinese families.

A baby was diagnosed with IFAP syndrome due to a new genetic mutation, showing severe skin and developmental issues.

A new mutation in the MBTPS2 gene causes a mild form of IFAP syndrome.

The cat's hypothyroidism was successfully managed with levothyroxine, leading to a stable condition.