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Overexpressing the mineralocorticoid receptor in mouse skin causes skin thinning, early skin barrier development, eye issues, and hair loss.

Dermoscopy helped diagnose a rare hair disorder in a 2-year-old boy.

A rare case links early-onset alopecia universalis and nephrotic syndrome, suggesting genetic immune issues.

MRI reveals thinner scalps and smaller hair follicles in people with androgenetic alopecia.

Sublingual minoxidil improved hair growth in a 10-year-old boy without side effects.

An 8-year-old girl with vitiligo developed extra hair growth on her knee after using tacrolimus ointment.

Certain miRNAs might be involved in a hair loss condition called frontal fibrosing alopecia and could possibly help in its diagnosis.

A boy with GAPO syndrome had hair loss similar to male pattern baldness without hormone issues, possibly due to skin or blood vessel problems.

A specific microRNA, chi-miR-30b-5p, slows down the growth of hair-related cells by affecting the CaMKIIδ gene in cashmere goats.

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

Children with pituitary dwarfism have higher zinc and copper, lower manganese, and similar iron levels in hair compared to normal children.

Follicular mucinosis in a 15-year-old is usually harmless but needs monitoring for possible lymphoma.

Scalp fungus infections in Spain are a health concern, with changing causes and a need for better treatment and prevention.

The man's scalp infection was treated successfully, and his hair grew back.

Biotin and acetazolamide improved hair and nail growth, mental function, and reduced headaches in a child with autism.

Cystic panfolliculoma is a rare, harmless tumor that can be confused with other skin tumors.

An 8-year-old Saudi boy was diagnosed with a rare genetic disorder causing hair loss, skin issues, and light sensitivity.

The scraggly mutation causes hair loss and skin defects in mice.

Pilomatricoma is a rare, benign skin tumor that requires surgical removal for best results.

Increased PPARGC1α relates to hair thinning in common baldness.

A newborn girl has a rare skin condition with two ulcers on her buttock that are healing on their own.

Alopecia in the woman was likely caused by vitamin A deficiency, not a fungal infection.

Becker's Melanosis and Hypertrichosis mainly affects young males, causing brown skin patches and extra hair on one side of the upper body.

Lack of Fgf21 slows hair growth by affecting gene interactions.

Monilethrix is a genetic hair disorder affecting hair shape, seen in two brothers.

Tinea capitis affects only a specific hair area, not deeper parts.

Neurosteroids in the brain can increase or decrease seizure risk in mice.

The scant hair in snthr-1Bao mice is likely caused by a deletion affecting the Plcd1 gene.

Frontal fibrosing alopecia is increasingly affecting men, causing hair loss around the hairline and possibly other areas.