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A new DSG4 gene mutation causes hair defects in a young girl.

New hair spray caused a hair shaft disorder.

Hair splitting and nail detachment are linked conditions.

A baby with maple syrup urine disease improved from skin problems by adjusting his diet to correct amino acid levels.

Lupus nephritis can cause severe kidney and blood vessel problems.

A rare ovarian tumor caused early puberty in a 3-year-old girl.

CAH requires a multidisciplinary approach, and while current treatments help, future therapies show promise.

Two patients with lupus had an unusual type of hair loss not typical for the disease.

The p.P25L mutation in the KRT5 gene causes a rare skin condition that worsens over time and may lead to hair loss starting in young adulthood.

Patients with lichen planus should be tested for hepatitis C.

People with Lichen sclerosus are more likely to have skin conditions like vitiligo and alopecia areata, heart disease risks, and other health issues. They should be checked for these, but screening plans shouldn't differ based on gender due to lack of data.

About 8% of people with systemic lupus erythematosus have chronic scarring alopecia, with certain symptoms and positive antibodies increasing the risk, while immunosuppressants may lower it.

A family showed a new condition with inherited hair loss and skin changes, possibly due to one genetic disorder.

Increasing isoleucine intake improved skin and health issues in an infant with maple syrup urine disease.

A patient with Satoyoshi syndrome improved with a treatment combining several medications, including carbamazepine and methotrexate.

The type of PCOS a woman has doesn't strongly predict her skin or metabolic symptoms; obesity is a more important factor.

A man with a rare adrenal cancer showed unusual symptoms and died four months after diagnosis.

An 8-year-old girl has a rare, irreversible hair loss condition caused by a genetic mutation.

Inherited ichthyoses cause widespread skin scaling and thickening due to gene mutations.

Zinc supplements improved symptoms in a Uyghur infant with a rare genetic disorder affecting zinc absorption.

Nevoid basal cell carcinomas start in the skin's top layer and hair follicles.

PCOS is linked to chronic low-grade inflammation, but the role of certain infections is unclear.

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

A woman with lupus had unusual symptoms like blisters, skin inflammation, and throat ulcers, which improved with steroid and dapsone treatment.

An infant with Hutchinson-Gilford Progeria Syndrome had successful surgery to fix breathing issues caused by a new genetic mutation.

Trichodysplasia spinulosa can occur after a heart transplant due to immunosuppressive drugs.

A woman's mature cystic teratoma caused her virilization by producing testosterone.

Sheehan's syndrome can sometimes cause psychosis.

Monilethrix is a genetic hair disorder causing fragile, beaded hair with no effective treatment.

A 3-year-old girl has short anagen syndrome, causing her hair to stay short.