Search

everythinglearnresearchcommunity

for

Search:↓

Natural products and phytochemicals may help with hair regrowth, but more research is needed.

A patient with a larger than usual genetic mutation had a broader range of symptoms for a muscle disease.

Researchers found a genetic link for hereditary hair loss but need more analysis to identify the exact gene.

Men with a family history of hair loss on their mother's side are more likely to have female pattern hair loss.

Accidentally eating a topical steroid may rarely cause acute generalized pustular psoriasis.

AGA can occur in children with family history; early diagnosis and treatment important.

Loose Anagen Hair Syndrome is a hereditary condition causing hair loss in children due to abnormal hair follicles.

Severe insulin resistance can be managed with medication, lifestyle changes, and treatment for related conditions.

Researchers found a gene mutation responsible for a rare hair loss condition.

Using SNP array testing helped quickly find the gene causing Woodhouse-Sakati syndrome in two related individuals.

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.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

Taking finasteride every other month can still help with hair loss but may be less effective over time compared to taking it daily.

Trilostane effectively treated hair loss in Alaskan Malamutes with no adverse effects.

DAVID syndrome is a condition with immune system and hormone deficiencies, needing early diagnosis to avoid serious complications.

Silastic-Dacron strips effectively prevent stretch-back after hair reduction surgeries.

Minoxidil foam effectively promotes hair growth and reduces hair loss in men.

PCOS and related metabolic issues often run in families.

Some children are born with unusually short, fine hair because their hair growth phase is short, but this often gets better by itself during puberty.

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

Estrogens are key for bone growth spurts in both boys and girls and affect growth into adulthood.

The document concludes that Hilary Mantel's memoir shows how childhood experiences affect adult health, criticizing modern medicine for ignoring the mental aspects of physical illness.

Hair loss improved with treatment and successful transplant.

Keratin proteins are crucial for hair structure and strength.

A specific gene variant is linked to heart disease, increased heart muscle, curly hair, and thick skin on palms and soles.

A girl inherited excessive body hair from her mother and grandmother.

A new mutation in the mitochondrial DNA was found in a boy with MELAS, even though his family didn't show typical signs.

KFSD is a rare condition causing scarring hair loss, with no effective treatment known at the time of the report.

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

Accurate diagnosis of pseudolymphomatous folliculitis is crucial to avoid mistaking it for more serious conditions.