Search

everythinglearnresearchcommunity

for

Search:↓

A boy with a rare form of early puberty caused by a new gene mutation responded well to treatment aimed at reducing testosterone and preserving adult height.

Using special RNA to target a mutant gene fixed hair problems in mice.

Trichoepitheliomas can be hard to distinguish from other skin conditions and often start in teenage years.

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.

A woman developed rare, unexplained curly hair on her scalp and eyelashes.

Children's hair loss can be caused by many factors, including autoimmune diseases, emotional stress, genetics, and infections, with treatment and prognosis varying.

The document concludes that a thorough history, physical exam, and specific tests are crucial for diagnosing and managing hair loss effectively.

A woman had 13 non-cancerous cysts on her scalp successfully removed in one surgery.

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

Twins had rare skin cysts likely due to genetics.

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

A young man was diagnosed with trichoepitheliomas, causing thick skin and hair loss.

Strong skin creams work well for long-term scalp inflammation in Rapp-Hodgkin Ectodermal Dysplasia.

Two specific SNPs in the TRPS1 gene cause excessive hair growth by altering the protein's structure.

A 4-year-old girl was diagnosed with erythrokeratodermia variabilis after other treatments failed.

Minoxidil treatment can stimulate hair growth in hairless puppies if applied early.

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

A rare skin disorder affecting the face was found in a 28-year-old Saudi man.

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

Hutchinson-Gilford Progeria Syndrome is a rare genetic disorder caused by a specific gene mutation, characterized by aging symptoms and managed by monitoring heart health and using low-dose aspirin.

Genetics, stress, and health issues can cause early hair greying, which affects self-esteem, and there's no cure, only hair dye.

A man had a benign pilar cyst on his face, which is rare and was successfully removed by surgery.

AGA, a common hair loss, is caused by genetics, hormones, age, and environmental factors.

A family was found with both Trichorhinophalangeal syndrome and Loose Anagen Syndrome, suggesting a genetic connection.

A Thai boy was diagnosed with a rare hair disorder causing hair thinning and shedding.

Scientists now better understand the genetics of hypohidrotic ectodermal dysplasia, leading to more accurate diagnoses and potential new treatments.

Researchers created a model to understand heart aging, highlighting key genes and pathways, and suggesting miR-208a as a potential heart attack biomarker.

Treating PCOS is complex, involving medication like metformin and lifestyle changes, and requires attention to mental health due to high depression and anxiety rates.

PCOS and related metabolic issues often run in families.

A woman with a new PTCH gene mutation has both Gorlin syndrome and severe hair loss.