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The S250C variant in a gene may cause autoimmunity and immunodeficiency by impairing protein function.

A new mutation in the HR gene causes hair loss in a specific family.

Women with non-classic congenital adrenal hyperplasia have higher risk for heart and metabolic problems.

Dermatoscopy is a useful tool for diagnosing hair disorders and can help choose samples for more detailed analysis.

A patient with steroid sulfatase deficiency had a unique hair pattern and a brain malformation not previously linked to the condition.

New treatments targeting specific genes show promise for treating keratin disorders.

Light microscopy is useful for diagnosing different hair disorders.

Hair restoration surgery can effectively increase pubic hair density, with patient satisfaction and natural results largely depending on the chosen hair pattern and graft design.

Baricitinib reduces inflammation and improves cell health in premature aging cells.

Men with more vanadium in their blood and who drink less soy milk are more likely to have hair loss.

The definition of Polycystic Ovary Syndrome may change with new research, and careful screening is key for managing the condition.

Siblings with signs of virilization should be tested for non-classical congenital adrenal hyperplasia, which does not affect adult height but may impact fertility and well-being if untreated.

Dihydrotestosterone treatment can help penis growth in boys with 5α-reductase deficiency but doesn't fully normalize size after puberty.

Tigason improved hair growth in a boy with monilethrix without side effects.

The most common cause of hair loss in children is tinea capitis, followed by alopecia areata and telogen effluvium.

Women experience various skin issues at different life stages, requiring careful treatment and awareness.

Erythromelanosis follicularis faciei can also affect women, though it's rare.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

WNT10A mutations cause varied symptoms in patients with odonto-onycho-dermal dysplasia.

A gene variant in KRT71 causes the curly fur in Selkirk Rex cats.

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

Two siblings had a rare immune disorder caused by a FOXN1 gene mutation.

WNT10A mutations often cause ectodermal dysplasias, with males showing more tooth issues than females.

Gene mutations can cause problems in male genital development.

The document concludes that accurate diagnosis of hair loss in children is crucial due to limited treatment options and the condition's psychological impact.

Managing PCOS effectively requires focusing on psychological health, lifestyle changes, and medication.

Future research on ectodysplasin should explore its role in diseases, stem cells, and evolution, and continue developing treatments for genetic disorders like hypohidrotic ectodermal dysplasia.

Hair loss in Androgenetic Alopecia is caused by genetics, aging, and lifestyle, leading to hair follicle shrinkage and related health risks.

Identifying nonclassic congenital adrenal hyperplasia and carriers of CYP21 mutations is challenging, and genetic counseling is recommended due to their prevalence.

Ovulation disorders are a major cause of infertility and menstrual problems in women.