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Patients with alopecia areata may have lower vitamin D levels than healthy people.

Congenital atrichia with papular lesions is often misdiagnosed, and new diagnostic criteria can improve accuracy.

The man's skin condition improved with sun protection and topical steroids, but UV exposure still caused flare-ups.

Early diagnosis and hormone therapy can significantly improve outcomes for post-partum pituitary insufficiency in resource-limited settings.

New mutations in the DSG4 gene cause a rare hair condition.

Older men's scalp damage increases with age and sun exposure, a baby girl in the Philippines has Schimmelpenning syndrome, and thyroid screening is advised for children with hair loss and certain risk factors.

The woman was diagnosed with Vogt–Koyanagi–Harada disease and successfully treated with medication, restoring her vision and stopping headaches.

The Thr1022Ala variant in the hairless gene is not a disease-causing mutation.

A gene mutation in mice causes increased mast cells and disorganized hair follicles in their skin.

The toddler's health issues were caused by too much vitamin A from supplements.

A genetic mutation in the LIPH gene causes tightly curled hair that stops growing in some Japanese individuals.

Inhibitors of 11β-HSD1 show potential for treating type 2 diabetes but require more testing for safety and effectiveness.

Bald thigh syndrome in sighthounds is caused by structural defects in hair shafts due to downregulated genes and proteins.

Vitamin B12 deficiency can cause facial dark spots that go away with treatment.

A toddler with a rash and developmental delays improved after treatment for severe malnutrition caused by a diet lacking in protein.

A gene mutation in mice causes hair loss, weak bones, and protein buildup, showing how protein processing issues can lead to diseases.

A specific gene mutation causes different hair defects in Indian monilethrix families.

Replacing defective mesenchymal cells with normal ones fixes thymic growth issues in 22q11.2DS mouse models.

Iron deficiency causes hair loss by affecting hair differentiation and cycling.

A genetic mutation in the EDA gene causes hypohidrotic ectodermal dysplasia in cats.

TTD patients don't have a higher skin cancer risk because their main issue is with transcription, not DNA repair.

The EDAR gene mutation leads to thinner and more deformed hair shafts.

ABCD1 gene mutations cause adrenomyeloneuropathy, leading to symptoms like limb weakness and spasticity, with management focusing on rehabilitation and spasticity treatment.

Different STUB1 gene mutations cause varied symptoms in autosomal recessive ataxias.

A new mutation in the AGPAT2 gene causes severe fat tissue loss and related health issues by reducing the protein's levels.

A Holstein calf in Iran with a severe genetic skin disorder was euthanized due to incurable symptoms.

Modified HDL can better deliver drugs and genes, potentially improving treatments and reducing side effects.

SLC3A2 is crucial for hair follicle stem cell function and hair growth.

Mutations in the DSG4 gene cause fragile, sparse hair in humans, mice, and rats.