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New gene discoveries have improved diagnosis and treatment for skin and hair disorders, but more research is needed to fully understand them.

About one-third of Saudi women with female pattern hair loss also have thinning hair at the back of their head.

Trichostasis spinulosa is a common but often unnoticed skin condition involving bundled vellus hairs, especially in people with darker skin or UV exposure.

Researchers found a new mutation in the HR gene causing hair loss and skin bumps in a Pakistani family.

A mutation in the KRT74 gene causes woolly hair by affecting hair texture.

The report concludes that atypical Brauer nevus is more common in males, present at birth, and often misdiagnosed due to its unusual scalp locations.

Certain hairstyles in an urban South African township are linked to specific scalp disorders.

Impulsiveness is common across various psychiatric disorders and linked to many psychological symptoms.

A six-year-old boy with excessive hair growth and other symptoms may have a genetic link on chromosome 17q, requiring regular medical follow-ups.

The article suggests renaming Polycystic Ovarian Syndrome (PCOS) to "Hyperandrogenic Persistent Ovulatory Dysfunction Syndrome" (HA-PODS) for accuracy and consistency, but no final decision was made.

The research confirms that Hidradenitis Suppurativa is characterized by increased inflammation, disrupted skin cell organization, and abnormal metabolic processes.

Researchers found genetic mutations causing hypohidrotic ectodermal dysplasia in 88% of studied patients and identified new mutations and genetic variations affecting the disease.

The document concludes that proper diagnosis and treatment of hair shaft disorders require understanding their unique causes and avoiding hair-damaging practices.

Metabolic syndrome linked to female hair loss; waist size and high blood pressure important factors.

Brownish halos around axillary hair can help diagnose frontal fibrosing alopecia.

Circadian rhythm disruption, chronic inflammation, hormones, metabolism, and genetics may increase prostate cancer risk.

Hirsutism is common among Iraqi women, often without a known cause, but family history is significant.

Frontal fibrosing alopecia in Bogotá mainly affects postmenopausal women, with possible links to hormonal changes and sunscreen use.

The research found that genetic factors for male pattern baldness in African men differ significantly from those in Europeans.

Genetic testing for hairless gene mutations is crucial to correctly diagnose and treat atrichia with papular lesions.

The Turkish version of the MAIA-2 Scale is valid and reliable for patients at a dermatology clinic.

A machine learning model can predict alopecia areata early using specific gene markers.

The HOXC13 gene affects different hair proteins in cashmere goats in varied ways and is controlled by a feedback loop and other factors.

The study suggests smoking is common in HS patients but its role is unclear, and more research is needed to understand HS causes.

Dystonia may be part of PAS-4 and linked to immune issues.

Social or cultural norms, not hair type, more likely influence how often people wash their hair.

Researchers found a gene mutation responsible for a rare hair loss condition.

Early and accurate diagnosis of congenital smooth muscle hamartomas is crucial to distinguish them from other conditions.

Early detection and multidisciplinary treatment are crucial for managing Papillon-Lefévre syndrome.

People with palmoplantar pustulosis, especially with bone issues, have different mouth bacteria compared to healthy people.