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

Ruxolitinib significantly improves multiple autoimmune conditions in APS-1 patients.

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

The document does not determine if adults with aphallia are fertile.

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

A Saudi girl was diagnosed with Loose Anagen Hair Syndrome, a rare condition causing easy hair loss without scarring.

Alopecia areata is an autoimmune condition causing hair loss, linked to genetic factors and immune system issues, with no cure yet.

The document is a detailed guide on skin conditions and treatments for dermatologists.

Alopecia in patients with epidermolysis bullosa varies in severity and is often caused by skin blistering or trauma.

The document concludes that various hair disorders have different treatments, including medication, surgery, and addressing underlying causes.

A rare endocrine disorder, APS 1, was diagnosed in a 26-year-old man in Bangladesh.

Using platelet growth factors can improve hair density in transplants, especially for those with fine hair.

Some skin conditions are associated with other serious diseases, and office microscopy may miss many fungal infections.

Keratosis Pilaris Atrophicans causes skin scarring and might be treated with a new synthetic retinoid.

In India, most patients with type 1 autoimmune polyglandular failure show symptoms in a specific order, starting with parathyroid gland issues, then yeast infections, and finally adrenal gland failure.

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

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

Clouston syndrome is inherited in an autosomal dominant pattern and caused by a specific gene mutation, with no current treatment available.

Controlling Tslp can improve health in AEC syndrome patients.

Different genes are linked to various types of hair loss.

Ectodysplasin signaling is crucial for skin appendage development, requiring specific doses and durations.

Growth factors greatly affect hair loss, with different levels seen in men, women, younger patients, and at the start of the condition.

Intense Pulse Light effectively reduces hair growth in faun tail nevus.

A specific genetic change in the KRT71 gene causes a hair loss condition in Hereford cattle.

A man had a large, rare cyst in his mouth removed after 10 years, which fixed his swallowing and breathing problems.

ASH2L is essential for skin and hair development.

Colorectal cancer development involves both genetic changes and epigenetic alterations like DNA methylation and microRNA changes.

Epidermolysis bullosa simplex causes easily blistered skin due to faulty skin cell proteins, leading to new treatment ideas.

Researchers created a mouse with the same mutation as humans with trichothiodystrophy, showing similar symptoms and confirming the condition is due to defects in DNA repair and gene activity.

HOXC13 is essential for hair and nail development by regulating Foxn1.