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The document concludes that doctors should recognize congenital triangular alopecia to avoid unnecessary treatments, as it does not respond to steroids like alopecia areata does.

The study found that pili bifurcati causes hair to intermittently split into two branches, each with its own outer layer.

Hair growth issues can be linked to genetics, diseases, or medications, and new treatments are being developed.

Congenital triangular alopecia is a harmless, non-spreading hair loss condition often seen in young children.

The document concludes that proper diagnosis and a multidisciplinary approach are crucial for managing Congenital Adrenal Hyperplasia effectively.

A woman got melanoma on her scalp after anti-hair loss treatment with injections.

Early adrenal gland maturation in young children can be normal, but other serious conditions should be ruled out first.

Oral isotretinoin temporarily improved skin symptoms in a child with IFAP syndrome.

LC-MS/MS is more reliable than immunoassays for diagnosing 21-hydroxylase deficiency.

Researchers found a new mutation in the FERMT1 gene in a Spanish family with Kindler syndrome.

New hair regrowth model introduced, imiquimod kills skin cancer cells, T-cadherin loss makes skin cancer more invasive, no strong link between PTCH1 gene and skin cancer after transplant, and male teens more likely to have hereditary hair loss.

The top research priorities for congenital ichthyosis include long-term side effects of oral retinoids, best topical treatments, and treatments for itch and hair loss.

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

Hirsutism in young girls can have various causes beyond PCOS, so diagnoses should be reconsidered if treatments don't work.

CAH is a genetic disorder affecting cortisol production and causing hormonal imbalances, with treatment and diagnosis varying by form and symptoms.

A 3-year-old boy was diagnosed with a rare, non-scarring hair loss condition called temporal triangular alopecia.

The study concluded that androstendione and DHEA are important for diagnosing high male hormone levels in women with excessive hair growth.

The review concludes that accurate diagnosis of different types of hair loss requires proper biopsy techniques and understanding the hair growth cycle and underlying causes.

Ovarian steroid cell tumors can mimic adrenal hyperplasia, and surgery can normalize hormone levels.

FOXN1 mutations cause severe immunodeficiency, hair loss, nail issues, and thymus defects.

Proper diagnosis and treatment of hair loss in children are crucial to prevent lasting issues and maintain their quality of life.

Two specific SNPs in the TRPS1 gene cause excessive hair growth by altering the protein's structure.

Hormonal imbalances in congenital adrenal hyperplasia cause acne.

A Korean boy's skin and digestive symptoms were caused by a rare genetic disorder that affects zinc absorption, and he got better with zinc supplements.

Hirsutism is mainly caused by high androgen levels or sensitivity, with PCOS being the most common cause.

Children with classic congenital adrenal hyperplasia have thicker heart fat and are at higher risk for heart problems and early atherosclerosis.

Netherton's syndrome is linked to high IgE levels and unique skin and hair symptoms, and may improve with ammonium lactate lotion and allergy management.

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

Micrografts and minigrafts are safe and effective for hair transplantation in facial and scalp reconstruction, providing high patient satisfaction.

A rare genetic mutation found in an Indian family can be detected through prenatal screening.