Search

everythinglearnresearchcommunity

for

Search:↓

Trichoscopy helps distinguish between scalp Discoid Lupus Erythematosus and Lichen Planopilaris for accurate diagnosis and treatment.

Cardiac risk markers help assess heart risk in males with type 2 diabetes and low DHT.

Specific keratin gene mutations can cause monilethrix.

LH and hCG reduce certain protein levels in women's skin.

The E413K mutation in the hHb6 gene causes monilethrix, a hair disorder, but doesn't show consistent symptoms.

The condition is linked to chromosome 12, but no mutations were found in the known genes.

Non-classical 21-hydroxylase deficiency can be missed in newborn screenings and should be considered in cases of early puberty or virilization.

A woman's severe hirsutism was caused by Leydig cell tumors in her ovaries, which improved after surgery.

Overexpression of HDGF in melanocytes does not cause cancer.

The document suggests that severe hair loss in SLE patients may be an early sign of scalp DLE, treatable with immunosuppressive therapy.

A new gene mutation causes vitamin D resistance and hair loss in two unrelated girls.

Idiopathic hirsutism may be linked to increased enzyme activity.

A gene mutation causes lanceolate hair in rats by disrupting hair shaft integrity.

Leydig cell tumors can cause hormone issues in postmenopausal women even if imaging looks normal.

Dermatologists should recognize diverse discoid lupus signs to avoid misdiagnosis.

3D-ultrasound can non-invasively detect and predict alopecia areata phases and outcomes.

A 13-year-old boy with a rare genetic condition survived a heart attack and improved with treatment.

The Lanceolate hair-J mutation in mice mimics human hair disorders like Netherton's syndrome.

Diagnosing and treating rapidly worsening lung disease is difficult and requires better guidelines and understanding.

Testing basal 17-HP levels is a good way to screen for nonclassic adrenal hyperplasia in women with high androgen levels.

Farudodstat may help treat alopecia areata by protecting hair follicles.

Blocking certain pathways with kinase inhibitors may help treat cutaneous lupus erythematosus.

Lipase H is important for hair follicle function and shaping hair fibers.

People with androgenetic alopecia may have higher cholesterol and triglycerides, suggesting a higher risk of heart disease.

Certain genetic changes in the LSS gene cause a rare skin and hair condition.

Boys with less severe EDA mutations in XLHED have milder symptoms and better sweat and hair production.

Combining medication and minimally invasive techniques can effectively manage Marine-Lenhart syndrome.

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