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A specific gene variant causes severe skin issues and increases infection risk, requiring careful medical monitoring.

A rare gene mutation causes skin fragility and itching without affecting hair or nails.

A specific gene mutation causes Olmsted syndrome.

Papillon-Lefèvre Syndrome causes early tooth loss and skin issues, needing early dental diagnosis.

A gene deletion in mice causes weak protein, immune issues, hair loss, airway problems, and wasting disease.

A mutation in the KRT71 gene causes a hair disorder by disrupting hair follicle structure and texture.

A new gene mutation causes hereditary coproporphyria with reduced enzyme activity.

Hair loss has many causes and treatments, and losing some hair daily is normal; proper diagnosis is key, and minoxidil can help treat it.

A new gene mutation causes vitamin D-resistant rickets and hair loss in two siblings.

A rare skin condition causes red and dark patches on the face and limbs.

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

PCOS is a common condition in women that causes various symptoms and health issues, treatable with lifestyle changes and medication.

Discoid Lupus Erythematosus often causes scarring hair loss, is influenced by genetics and environment, and requires early treatment to prevent worsening.

Progeria, a disease that causes early aging, is linked to a gene mutation and helps us understand normal aging.

The absence of functional sebaceous glands causes hair follicle destruction and scarring alopecia.

A different gene near the hairless gene on chromosome 8p21 causes a rare hair loss condition in a German family.

A mutation in the EDNRA gene causes Oro-Oto-Cardiac syndrome, affecting face and heart development.

The p.P25L mutation in the KRT5 gene causes a rare skin condition that worsens over time and may lead to hair loss starting in young adulthood.

Removing a specific gene in certain skin cells causes hair loss on the body by disrupting normal hair development.

Multi-omics techniques help understand the molecular causes of androgenetic alopecia.

An infant with complete hair loss was diagnosed with a genetic disorder affecting hair growth.

The document concludes that better treatments for CCCA are needed and more research is required to understand its causes related to hairstyling and genetics.

The conclusion suggests a new way to classify bradykinin-mediated angio-oedema based on different causes and its possible link with urticaria, which could improve diagnosis and treatment.

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

Polycystic Ovarian Syndrome (PCOS) is a common condition causing fertility issues and other symptoms, with unclear causes and treatments focused on improving insulin sensitivity.

Melanoma risk tools need improvement, a gene mutation causes a hair disorder that might be treated by managing cell stress, a potential therapy for a skin-ear disorder involves blocking cell channels, skin wrinkling may indicate lung aging regardless of smoking, and oxidative stress might contribute to common baldness.

Pili torti is a rare condition where hair is twisted and breaks easily, often linked to genetic disorders or other health issues.

A woman with a rare hormone resistance condition also had missing teeth and hair loss, which might be new symptoms of her genetic disorder.

Any medication can cause skin reactions, some due to allergies and others due to dosage or genetic factors.

The document concludes that hair loss is complex, affects many people, has limited treatments, and requires more research on its causes and psychological impact.