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A protein called ectodysplasin-A2 increases a hair growth inhibitor in balding cells, which could be a target for hair loss treatment.

CD2 might be a new treatment target for patchy alopecia areata.

Twins had rare skin cysts likely due to genetics.

A patient with total hair loss developed vitiligo after using a treatment called DCP.

Researchers found a new mutation in the HR gene linked to a rare hair loss condition.

Topical PUVA and tacrolimus ointment can effectively and safely treat infant alopecia universalis.

Hairless mammals have genetic changes in both their protein-coding and regulatory sequences related to hair.

MendelVar is a tool that helps identify important genes by combining GWAS data with Mendelian disease information.

Biotin supplements are unnecessary for most people but may help with certain conditions like biotin deficiency, brittle nails, and some hair loss.

Telogen Effluvium is a common hair loss condition, particularly in women, with no specific FDA-approved treatment, and recovery can take up to 18 months.

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

Understanding skin structure and development helps diagnose and treat skin disorders.

The baby’s hair loss was due to a rare genetic condition, not treatable by usual methods.

Genetic testing confirmed a young girl has Atrichia with Papular Lesions due to mutations in the hairless gene.

Uncombable hair syndrome causes frizzy hair and can affect the nervous system, eyes, and ears, often co-occurring with other hair, skin, nail, and teeth conditions, and is linked to three specific gene mutations.

A 37-year-old male with severe skin and internal issues has a rare inherited skin condition called dystrophic epidermolysis bullosa.

The most common cause of hair loss in children is tinea capitis, followed by alopecia areata and telogen effluvium.

An 8-year-old girl had nail and hair issues that improved without specific treatment, but fungal nail infection was hard to cure.

The document reports unique growth lines in a child after Stevens-Johnson syndrome, skin reaction from parsnips and sun in a girl, and itchy skin with xanthomas in a boy with Alagille syndrome.

Hormone treatment caused hair loss, finasteride helped regrowth.

Atopic dermatitis may have genetic causes and can be treated with pharmacologic methods, glycerin creams, and controlling Staphylococcus aureus colonization.

Mutations in three genes cause Uncombable Hair Syndrome, leading to frizzy hair that can't be combed flat.

Minoxidil is used to treat hair loss.

A child with Olmsted syndrome showed mild improvement in hair and skin issues with treatment.

Human hair keratins K85 and K35 create unique filament patterns important for early hair formation.

Edar signaling is crucial for controlling hair growth and regression.

Genetic changes in mice help understand skin and hair disorders, aiding treatment development for acne and hair loss.

A person was born with both a rare hairless condition and a type of birthmark, which is an uncommon combination.

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