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Uterine leiomyomas don't significantly change gene expression in the scalp of people with Central Centrifugal Cicatricial Alopecia.

Long-term use of androgens can help manage Hereditary Angioedema (HAE) but may cause serious side effects, so alternative treatments with fewer side effects are being considered.

The protein FLCN is involved in cellular cleanup and is regulated by ULK1.

PCOS is a condition causing irregular periods, excess male hormones, and infertility, often managed by targeting insulin resistance and specific symptoms.

A baby was diagnosed with IFAP syndrome due to a new genetic mutation, showing severe skin and developmental issues.

A woman with lupus had muscle weakness due to kidney issues and was successfully treated with medication.

Nanostructured delivery systems could potentially improve hair loss treatment by targeting drugs to hair follicles, reducing side effects and dosage, but the best size, charge, and materials for these systems need further investigation.

Trichoscopy helps tell apart Frontal Fibrosing Alopecia and Lichen planopilaris by showing different hair and scalp features.

A TP63 gene mutation causes significant hair loss and mild skin, nail, and tooth abnormalities.

A person got uncombable hair syndrome from two copies of chromosome 1 from their mother.

Exosome treatment safely increases hair density in male patients with androgenetic alopecia.

Vitamin D is important for skin health and can help treat psoriasis, atopic dermatitis, and vitiligo.

FGF13 gene changes cause excessive hair growth in a rare condition.

A new genetic mutation in the ODC1 gene causes developmental delay and other symptoms in a young girl.

Hair graying may be caused by stem cell depletion from stress or melanocyte damage.

Nilotinib can cause keratosis pilaris, a skin condition.

Genetics and nutritional deficiencies are key factors in premature graying of hair.

Dermoscopy helps accurately diagnose temporal triangular alopecia, avoiding unnecessary treatments.

Melasma's causes include genetics, sun exposure, hormones, and oxidative stress, and understanding these can help create better treatments.

A boy's skin fragility and sparse hair were caused by a genetic mutation affecting skin cell adhesion.

Nilotinib can cause generalized keratosis pilaris.

The document concludes that while white skin, nail, and mucosa diseases increase skin cancer risk, they are generally harmless, especially compared to darker pigmentation conditions.

A person was born with both a rare hairless condition and a type of birthmark, which is an uncommon combination.

DAVID syndrome is a condition with immune system and hormone deficiencies, needing early diagnosis to avoid serious complications.

Botulinum toxin injections effectively relieve pain from cutaneous leiomyomas.

A rare genetic mutation caused unusual skin symptoms in a man with Blau syndrome.

The woman has a rare skin condition called follicular Dowling-Degos disease, which has limited treatment options.

A baby had a rare case of widespread milia, which was treated and is being monitored.

A cat's poor wound healing was linked to a genetic deletion in the COL5A1 gene.

Protein analysis shows aging changes in scalp cell types from women.