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New ABCA12 gene mutations were linked to a skin condition with scaling and hair loss, and a treatment helped with hair loss in a related case.

Infectious cerebral vasculitis can be a severe complication of meningoencephalitis, regardless of the pathogen.

ABCD1 gene mutations cause adrenomyeloneuropathy, leading to symptoms like limb weakness and spasticity, with management focusing on rehabilitation and spasticity treatment.

Loss of Msx2 function causes eye development issues similar to Peters anomaly.

A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.

The document adds two cases of Gomez-Lopez-Hernandez syndrome and suggests including trigeminal anesthesia and scalp alopecia as key diagnostic criteria.

A girl with a rare syndrome had successful hair loss treatment with no relapse after 4 years.

LC-OCT helps accurately diagnose different types of infant hair loss without invasive methods.

Skin lesions in Carney Complex are caused by a gene change in some skin cells that leads to increased pigmentation and may lead to tumors.

A severe form of Netherton syndrome caused by a specific gene mutation led to neonatal deaths in a family.

Tissue-specific variation in mutant load complicates genetic counseling and prenatal diagnosis.

A new AIRE gene mutation causes rare autoimmune symptoms in a Lebanese boy.

Combination therapy of doxazosin and finasteride safely and effectively reduces benign prostatic hyperplasia progression risk.

Finasteride reduces urinary issues and surgery need in men with enlarged prostates by over 50%.

Finasteride doesn't harm male fertility or sperm quality, but may slightly reduce ejaculate volume.

A new method accurately classifies hair types, showing global hair diversity.

Human hair can be classified into eight types based on physical features, not ethnicity.

Hair ages as the cuticle wears down, especially beyond 1 meter from the root, affecting its strength and shine.

Antimicrobial lotion reduces inflammation and increases hair density in hair loss patients.

Hair growth and shedding are linked and can be disrupted, causing a delay known as the hair eclipse phenomenon, which is common in certain hair conditions and could lead to new treatments.

Finasteride daily doesn't affect sperm production or semen in young men.

ATR04-484 ointment shows promise for treating skin issues from cancer therapies.

ATR12-351 ointment safely delivers LEKTI protein to the skin, reducing enzyme activity in Netherton syndrome.

A 7-year-old girl had unusually long eyelashes with no known cause or related health issues.

A new ARID1B gene variation causes Coffin-Siris syndrome 1 and early high myopia in a Chinese family.

A U.S. Naval fighter pilot suffered permanent vision loss in one eye due to recurrent central serous retinopathy.

A 14-year-old girl's black hair showed unique color changes, suggesting early greying.

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