Search

everythinglearnresearchcommunity

for

Search:↓

A new genetic variant in the LIPH gene causes hair growth issues in a Chinese patient.

Satoyoshi Syndrome is hard to diagnose and treat due to its rarity and complex symptoms.

An infant with a zinc deficiency skin disorder improved with zinc treatment.

Atrichia with papular lesions causes irreversible hair loss from infancy and is often misdiagnosed.

Accurate diagnosis of APL is crucial to avoid unnecessary treatments.

A rare gene mutation causes skin fragility and itching without affecting hair or nails.

The document concludes that Rabson-Mendenhall syndrome requires novel treatments for insulin resistance and emphasizes the importance of dental care in affected patients.

Combining ciclosporin and simvastatin can cause severe kidney damage.

Researchers found a new mutation in the HR gene causing hair loss and skin bumps in a Pakistani family.

Stopping valproate and using lactulose can quickly treat valproate-induced hyperammonemia.

Certain gene variations may increase the risk of hair loss in Egyptians.

Abrocitinib may effectively treat stubborn alopecia universalis.

Genetic variants in specific genes cause central centrifugal cicatricial alopecia.

A 69-year-old man with sinus infection and fainting spells was diagnosed with a rare kidney disease, treated with steroids and a specific drug, which improved his condition.

Two new enzymes, PAD-R11 and PAD-R4, were cloned and showed activity, with PAD-R11 resembling epidermal enzymes.

5α reductase type 2 enzyme mutation and oxidative stress may increase androgenetic alopecia risk in Egyptians.

Acitretin helped improve hand mobility and skin condition in a patient.

Lower nitric oxide and higher fibrinogen found in hirsute women; impaired sexual function in 22.6% of hair loss patients, linked to psoriasis severity.

Some women with excess hair growth have a hormone condition that can't be diagnosed by blood or urine tests alone.

An infant with seizures and hair loss was diagnosed with biotinidase deficiency and treated successfully with biotin.

Men with X-linked recessive ichthyosis can still experience male-pattern baldness.

Certain genetic variations can make people more likely to experience hair loss and low white blood cell count from azathioprine.

Certain gene variations and low adiponectin levels may increase the risk of hair loss in Egyptians.

A woman with lupus also developed a severe skin condition linked to a genetic factor.

New niosomal formulation effectively delivers aminexil through rat skin.

Oral zinc therapy is effective for treating acrodermatitis enteropathica.

Alopecia areata may be linked to kidney issues, but more research is needed.

Cantú syndrome may be linked to pituitary adenomas.

Azathioprine treatment led to rapid hair regrowth in a woman with alopecia universalis.