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SA linked to mitochondrial issues and oxidative stress, while AGA involves disrupted hair growth genes.

Rectangular black granules, solitary yellow dots, and mostly single-hair follicles suggest Loose Anagen Hair Syndrome.

Stopping tight hairstyles can prevent and reduce traction alopecia.

The document concludes that identifying the cause of eyebrow and eyelash loss is key to treating it and improving quality of life.

Poliosis circumscripta is a patch of white hair caused by lack of melanin, linked to genetic and acquired conditions.

Gomez–Lopez–Hernandez syndrome can cause focal hair loss and developmental delays but some children can still function well and excel in school and sports.

A girl with a rare syndrome had successful hair loss treatment with no relapse after 4 years.

Many hair loss conditions can be treated.

Up to 50% of scalp hair can be lost before it appears thin, and treatment is only needed for hair loss caused by diseases or deficiencies.

Researchers found new hair and nail genes, how hair reacts to UV, differences in white and pigmented hair growth, nerve changes in alopecia, treatments for baldness and alopecia, a toenail condition linked to a genetic disorder, and that nail fungus is more common in people with psoriasis.

Netherton syndrome can cause severe dehydration, infections, and growth issues in infants.

Different types of hair loss require specific treatments, and new treatments are being developed.

Children's hair loss can be caused by many factors, including autoimmune diseases, emotional stress, genetics, and infections, with treatment and prognosis varying.

Hair transplantation between identical twins can successfully treat severe, nonprogressive hair loss due to follicular aplasia.

A Chinese man with KID syndrome had a new mutation in the GJB2 gene.

A Korean girl developed kinky hair without known cause or effective treatment.

A woman's hair changed to a dry, tangled texture that's hard to comb after treatment with spironolactone, suggesting the medication might cause such hair changes.

The document concludes that early diagnosis and treatment are crucial for children with hair loss to prevent permanent damage, although not all conditions can be effectively treated.

The document concludes that understanding hair biology and recognizing hair conditions are crucial for managing and treating hair loss in children.

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

Some congenital hair disorders improve with age and can be managed with treatments like minoxidil, retinoids, supplements, and gentle hair care, but there's no cure.

Some congenital hair disorders improve in childhood or with treatments like minoxidil and retinoids, while others like Netherton syndrome and trichothiodystrophy have a poor prognosis.

The document emphasizes the importance of correctly identifying and classifying genetic hair disorders to help diagnose related health conditions.

Some scalp sores are linked to different inherited skin conditions.

Mutations in the DSG4 gene can cause a rare hair disorder similar to monilethrix.

Nonclassic congenital adrenal hyperplasia is a genetic disorder causing hormone imbalances, affecting fertility and requiring personalized treatment.

Non-classic congenital adrenal hyperplasia is a common disorder causing symptoms like acne and infertility, and it's managed based on symptoms, not just test results. Treatment can improve fertility and reduce miscarriage risk.

A boy had unusual synchronized hair growth with short active growth phases, not fitting known hair disorders.

European guidelines recommend regular eye and ear exams, skin care, vitamin D supplements, and cautious use of medications for managing congenital ichthyoses.

Quick treatment of hair disorders in teenage girls is important because of the emotional effects.