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An 8-year-old Saudi boy was diagnosed with a rare genetic disorder causing hair loss, skin issues, and light sensitivity.

PCOS often causes skin issues like excess hair, acne, and hair loss, needing early treatment.

The girl's regrown brown hair had less of certain pigments than her original black hair.

A 2-year-old boy grew excessive hair after using minoxidil for hair loss, but it improved when the treatment stopped.

Minoxidil works better for female hair loss, but cyproterone reduces scalp oiliness and causes menstrual issues.

Some children are born with unusually short, fine hair because their hair growth phase is short, but this often gets better by itself during puberty.

New mutations in MBTPS2 reduce its function and cause IFAP syndrome with unusual symptoms.

The conclusion is that young women with excessive hair growth should be quickly tested for hormonal issues and treated to improve their social well-being.

AGA is a genetic, hormonal hair loss treated with finasteride, minoxidil, and supplements, but new compounds are being developed.

A woman with a rare scalp lymphoma had unusual hair loss after treatment.

The document reports three sisters with Woodhouse-Sakati syndrome showing typical symptoms and unusual gynecological anomalies.

Melatonin-loaded microemulsion could be a promising treatment for hair loss.

Myotonic dystrophy should be considered in patients with hair thinning, and genetic counseling is important.

Mutations in the WNT10A gene can cause skin, hair, teeth, and other disorders, and may also affect other areas like kidney and cancer, with potential for targeted treatments.

Vitamin D is important for bones, hair, blood pressure, and breast development.

Some autistic children may have higher levels of male hormones, which could be linked to aggression.

The review shows how to properly diagnose and treat the loss of eyebrow and eyelash hair.

A rare skin condition with dark, thick, warty patches and some hair loss was found in a newborn boy.

A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.

A new genetic change in the DSC3 gene is linked to a rare condition causing hair loss and skin blisters in a child.

Male genital development is driven by androgen signaling and understanding it could help address congenital anomalies.

Men with androgenetic alopecia, or hair loss, often have abnormal blood flow in their small blood vessels, which might be linked to inflammation and stress.

A boy with chromosome 13q deletion syndrome developed eye cancer, a woman with breast cancer lost vision due to a rare side-effect of her treatment, a man's vision worsened after using a hair loss drug, and two rare disorders were discussed. Optical Coherence Tomography is useful for diagnosing and monitoring these conditions.

Various surgical techniques effectively treat skin diseases and cosmetic issues.

High androgen levels and genetic factors likely cause Becker's nevus and related symptoms.

Treatment reduced cystic lesions but didn't change existing Nevus Comedonicus.

Society's view of "freaks" has shifted from natural deformities to extreme plastic surgery, reflecting changing beauty standards and pressures.

Ring Chromosome 11 may be linked to conditions like early puberty, excessive hair growth, hair loss, and type 2 diabetes.

The document concludes that careful diagnosis is crucial for chromosome 13q deletion syndrome, tamoxifen can cause reversible eye damage, finasteride may be linked to cataracts, and OCT is useful for diagnosing macular diseases.

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