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The Swedish neonatal screening program effectively detects PKU, galactosaemia, and biotinidase deficiency with low false positives.

Compound 6 is a promising candidate for better wound healing.

Long COVID is a big health problem needing more research and better treatments.

A new genetic mutation causing Xeroderma Pigmentosum was found in an 8-year-old girl, affecting her DNA repair.

Baricitinib successfully regrew hair in an 8-year-old boy with alopecia totalis linked to a KRT74 gene variant.

Follicular vitiligo causes hair to gray without skin color loss.

A rare hair follicle disorder can cause itchy, bluish-black bumps on the body.

The document concludes that "hot comb alopecia" is now called "central cicatricial centrifugal alopecia" and its causes are complex.

Patients with a specific genetic variant have more severe alopecia areata and higher recurrence rates.

Two gene areas linked to male pattern baldness found, more research needed.

Food intake, not genetics, affects how the body processes tadalafil and finasteride.

Histopathology is crucial for accurately diagnosing and predicting outcomes of skin adnexal tumors.

COVID-19 may cause hair loss, often after recovery, with androgenetic alopecia being the most common type.

Neutrophils quickly respond to skin injury.

Nonmelanoma skin cancers have higher levels of certain osteopontin variants than normal skin.

A woman with dermatomyositis showed rare skin symptoms, was treated successfully, and her case suggests checking for cancer in similar patients.

HLA-DRB5 and other genes may be linked to alopecia universalis.

Alopecia areata and vitiligo can coexist, respond well to treatment, and may have a better prognosis together.

A woman with a rare type of dermatomyositis improved with low-dose prednisone and methotrexate.

The family has a unique form of ectodermal dysplasia similar to Clouston syndrome but with different hair and skin symptoms.

Elderly men with a scalp condition healed in about 26 days using specific creams and dressings, with no return of the condition in 6 months.

OsUEV1B protein is essential for controlling phosphate levels in rice.

Two siblings have a rare hair condition caused by a new genetic variant.

COVID-19 and vaccines cause various skin reactions and highlight the need for dermatologists in managing these issues and addressing vaccine distribution disparities.

Live vaccines can be safely given to infants with a FOXN1 variant if their immune function improves over time.

Lichen planus on the scalp can cause scarring hair loss and has four main types.

Genetic testing can diagnose hair loss linked to DSG4 gene variants.

A girl with Becker naevus syndrome has a genetic variant in the ACTB gene related to her symptoms.