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Male-pattern hair loss is largely influenced by genetics, with key genes identified.

The study found that Keratosis Pilaris Atrophicans is a genetic skin condition that starts in childhood, involves inflammation and scarring, and current treatments are only somewhat effective.

Some people have genetic mutations that make them resistant to vitamin D, leading to rickets even with enough vitamin D intake.

The research suggests that the global distribution of PCOS is likely due to historical human migration and that genes affecting PCOS may have different impacts on males and females.

Buschke-Ollendorff syndrome is a rare genetic disorder causing skin and bone changes, with some cases also showing ADHD or developmental delays.

Polycystic ovarian shape is a genetic sign of PCOS and its hormonal and metabolic features can be inherited.

A mother and son both had ulcerative colitis and alopecia, suggesting a genetic link in autoimmune disorders and successful treatment with cyclosporine.

Leech therapy and Ayurvedic treatment can effectively regrow hair in recent Alopecia areata cases.

Genomic profiling for myeloid cancers can find important inherited mutations, but it's challenging when these mutations aren't related to the patient's symptoms.

Minoxidil improves blood flow and vessel flexibility, potentially helping with vascular stiffness.

Twins had rare skin cysts likely due to genetics.

Cronkhite-Canada syndrome can sometimes show unusual colonic adenomatous polyps.

Diphencyprone can cause unexpected and possibly permanent vitiligo.

Patients with GATA2 deficiency show early skin symptoms that help diagnose the condition.

PCOS is a common hormonal disorder in women that can affect skin, fertility, and metabolism, and treatment is tailored to individual needs.

New treatments for excessive hair growth in women include insulin modulators and enzyme inhibitors.

A specific gene mutation causes Olmsted syndrome.

The combined treatment effectively managed severe skin issues in Olmsted syndrome.

Some women with PCOS have CYP21 mutations and IRS1 variants, but these genetic factors are not major contributors to PCOS.

Primary idiopathic pseudopelade of Brocq causes gradual, scarring hair loss with no effective treatment.

The patient with total hair loss did not regrow hair despite treatment, indicating a poor outlook for this type of hair loss.

Frontal fibrosing alopecia causes hair loss at the front hairline, and no effective treatment exists.

A 25-year-old man with multiple skin tumors was successfully treated with acitretin and methotrexate.

Kids with early graying hair often have low levels of calcium, ferritin, and vitamin D3.

FGF5 gene mutations cause unusually long eyelashes by affecting hair growth regulation.

Genetic testing is crucial for diagnosing rare hair loss disorders.

The study found that horizontal sections of scalp biopsies are better for analyzing hair loss, showing fewer hairs and more fine hairs in balding areas.

The study found that polymorphous light eruption varies among patients and can be distinguished from benign summer light eruption by the time it takes for symptoms to appear after sun exposure.

Minoxidil effectively promotes hair regrowth in younger patients with small balding areas.

KCNQ potassium channels help control the sensitivity of touch receptors in the skin.