Search

everythinglearnresearchcommunity

for

Search:↓

Hair loss in black women needs more research, early intervention, and community education.

The document concludes that understanding the genes and pathways involved in hair growth is crucial for developing treatments for hair diseases.

Two siblings were the first reported cases of inheriting both eye coloboma and loose anagen syndrome together.

A rare genetic skin condition usually affecting males was found in a 9-year-old girl.

Genetic mutations cause various hair diseases, and whole genome sequencing may reveal more about these conditions.

A one-year-old child with a genetic condition had symptoms improved by treating zinc deficiency.

An 8-year-old girl has a rare, irreversible hair loss condition caused by a genetic mutation.

Genes and hormones cause hair loss, with four genes contributing equally.

The study found no common cause for a girl's crystalline cataract and uncombable hair, suggesting their co-occurrence might be coincidental.

The document concludes that AFA should be considered in patients with acromegaly-like features but normal hormone levels, and more cases need to be identified to understand the condition fully.

There is no cure for myotonic dystrophy type 1, so treatment focuses on managing symptoms and complications.

Cantú syndrome is caused by mutations in the ABCC9 gene.

Loose Anagen Hair Syndrome is found in black-haired Indian children and is often missed, especially in boys.

The EDAR gene mutation leads to thinner and more deformed hair shafts.

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

A new genetic area linked to a rare hair loss condition was found on chromosome 13 in a Chinese family.

Treatment with plasma rich in growth factors improved hair density and thickness for hair loss patients.

The document concludes that hair transplantation and gene therapy may be important for future hair loss treatment.

The document concludes that better treatments for CCCA are needed and more research is required to understand its causes related to hairstyling and genetics.

Metformin taken during pregnancy increases SHBG in newborns but doesn't change other hormone levels in mothers or babies.

Longer hair loss leads to more severe CCCA; early treatment and avoiding damaging hairstyles help regrowth.

Women experience various skin issues at different life stages, requiring careful treatment and awareness.

The document emphasizes the importance of correctly identifying and classifying genetic hair disorders to help diagnose related health conditions.

A Turkish family with sparse hair and eyebrow loss has a mutation in the U2HR gene linked to Marie Unna hereditary hypotrichosis.

Male pattern baldness is often genetic and linked to a hormone, with treatments like finasteride and minoxidil being effective for some men.

A new gene location for Keratosis follicularis squamosa was found on chromosome 7p14.3-7p12.1.

A man's baldness improved possibly due to a medication that blocks male hormones.

Ayurvedic treatment helped reduce PCOS symptoms in a 19-year-old girl.

Skin lesions in Carney complex are likely caused by a specific group of skin cells that promote pigment production due to a genetic mutation.

A Saudi girl was diagnosed with Loose Anagen Hair Syndrome, a rare condition causing easy hair loss without scarring.