Search

everythinglearnresearchcommunity

for

Search:↓

Two unusual cases showed that Lichen Planopilaris can look like other skin conditions and need early treatment to protect hair.

Hutchinson-Gilford Progeria Syndrome causes rapid aging from a genetic mutation, with no cure but ongoing research into potential treatments.

Some children in Malaysia with symptoms have either profound or partial biotinidase deficiency, and early testing and treatment are important.

Gorillas in Gabon improved after protein supplements were added to their diet.

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

A young man with an unusual type of scarring hair loss suggests a possible new variant of a known scalp condition.

Mitochondrial dysfunction and oxidative stress may play a role in Lichen Planopilaris.

Increased blood vessel growth in lichen planopilaris may signal active disease needing aggressive treatment.

RY-023, a specific drug, can improve early stage memory learning without affecting general activity in rats, but it's less effective for later learning stages and doesn't impact memory recall.

The conclusion is that FFA and LPP have similar scalp biopsy features, making them hard to distinguish histologically, and FFA may be a specific kind of scarring hair loss.

Lichen planopilaris causes permanent hair loss and scarring due to damage to hair follicles and can be mistaken for other hair loss conditions.

Most elderly patients in Benghazi have skin diseases, mainly fungal infections.

Flexural follicular lichen planus is a rare skin condition affecting body folds.

The conclusion is that certain scalp tissue changes are characteristic of lichen planopilaris, with mucinous perifollicular fibroplasia being a new feature for diagnosis.

Some overweight or obese men with long-term frontal fibrosing alopecia may have abnormal sex hormone levels.

PEH in vulvar LS is common and needs careful diagnosis to avoid confusion with cancer.

Early recognition of loose anagen hair syndrome is important to prevent misdiagnosis and unnecessary treatments.

Isolated patchy heterochromia with pili annulati can occur without other health issues.

A woman's new seizures were caused by a brain tumor likely linked to her past cancer treatment, and choosing safe seizure medications is important for women who can have children.

A 4-year-old had a rare type of hair loss that may have a good outcome.

A 13-year-old girl was diagnosed with juvenile lupus, showing only hair loss as a symptom.

Researchers created a new mouse model for studying Citrullinemia Type I and similar conditions, showing symptoms and treatment responses like those in humans.

Every elderly patient had at least one skin condition, often linked to other diseases, highlighting the need for integrated skin and general healthcare in the elderly.

Dermoscopy is useful for diagnosing and monitoring discoid lupus erythematosus by showing specific skin patterns.

Woolly hair is a rare genetic condition with no effective treatments.

PCS rats show significant inner ear damage and zinc deficiency, similar to liver cirrhosis patients.

Accurate diagnosis of NLS with dilated hair follicles is crucial to distinguish it from other conditions.

A Japanese patient with IFAP syndrome had a severe MBTPS2 gene mutation but showed milder symptoms than previously observed cases.

A mutation in mice causes hair loss and skin issues due to a defect in a gene affecting cell adhesion.