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Psoriasis on the scalp causes smaller oil glands and thinner hair but doesn't lead to hair loss.

The Oat mouse model shows mild retinal degeneration, useful for testing treatments.

Scientists found a new protein, AMY117, common in Alzheimer's patients, which could be important for treatment and diagnosis.

HLD10 can include increased body hair and Mongolian spots.

Hair loss can indicate brain aging and potential small vessel disease, but more research is needed to understand the clinical impact.

A woman's unique dementia was misdiagnosed, a genetic mutation increases Parkinson's risk with age, and finasteride may help with Tourette syndrome.

MRI can show unusual brain changes in adrenomyeloneuropathy.

The research found that a specific gene mutation causes fewer hair follicles and disrupted hair growth cycles, leading to thin and short hair in people with Hypotrichosis with Juvenile Macular Dystrophy.

Advanced male pattern baldness affects the back of the scalp, reducing hair follicles.

A 2-year-old boy with a rare brain malformation may have Gomez–López-Hernández syndrome.

The HtrA1L364P mutation causes brain dysfunction and blood vessel damage.

The new delivery system improves Alzheimer's symptoms by releasing Huperzine A slowly and effectively.

THA is a rare condition with no significant clinical consequences if thyroid function is normal.

A rare genetic disorder causes sparse hair and vision loss due to a CDH3 gene mutation.

H1 increases risk for neurodegenerative diseases, while H2 offers protection but is linked to other disorders.

Hyaluronate fragments can help reverse skin thinning by working with the CD44 receptor.

CDH3-related disease causes worsening eye and hair issues.

A dog had a rare skin condition linked to gland and pituitary issues.

A young Caucasian man experienced a rare type of hair loss on the back of his head.

Lipedematous alopecia causes permanent hair loss due to increased scalp fat.

Shrinking of oil glands in the skin is a key sign of hair loss linked to TNF inhibitor drugs and may improve if the treatment is stopped.

A deletion in the CDH3 gene causes a rare disorder with short hair and vision loss.

Gomez–Lopez–Hernandez syndrome can cause focal hair loss and developmental delays but some children can still function well and excel in school and sports.

Postmenopausal women may experience frontal hairline and eyebrow loss due to cicatricial fibrosis.

Friedreich's ataxia causes thin, weak hair with surface damage and cavities.

Dilated pupils can be an early sign of HIV/AIDS.

An 11-month-old boy with Menkes disease had severe brain shrinkage and abnormal blood vessels, and didn't respond well to treatment.

A heterozygous mutation in HTRA1 can cause severe CARASIL symptoms.

A rare genetic disease causes sparse hair and early blindness due to a gene mutation.

Thalamic stroke can cause delirium without other symptoms, especially in older adults.