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The document concludes that managing non-classical congenital adrenal hyperplasia in females requires personalized treatment, genetic counseling, and a team of specialists.

Hepatitis C virus can cause skin diseases and dermatologists play a crucial role in identifying these conditions.

Mutations in the HEPHL1 gene cause abnormal hair and cognitive issues.

Finasteride effectively treats enlarged prostate and male baldness, improves symptoms of hirsutism in women, but doesn't work for acne, and may delay prostate cancer progression with few side effects.

Identical twins had different symptoms because one had more cells with an extra chromosome fragment in different tissues.

The study found that hair fragility in Pili annulati may be caused by cavities and damage within the hair shafts.

Epidermolytic ichthyosis can be inherited in a semidominant way with mild symptoms in carriers.

The article helps identify common, non-harmful skin conditions in newborns to avoid undue concern and treatment.

Wharton's jelly-derived stem cells were safely used to treat four alopecia patients, resulting in hair regrowth in all of them.

Finasteride use during early pregnancy may cause limb deformities in babies.

A preterm baby's toes were saved from damage by quickly removing a thread that was cutting off circulation.

A child used a hair growth lotion for hair loss, but it caused excessive hair growth on his face and neck instead.

A woman with unexplained hair loss was found to have harmless skin tumors and a scarring hair loss condition, but the tumors didn't cause the hair loss.

Syphilis is becoming more common and remains a major health problem due to challenges in prevention and treatment.

A heterozygous mutation in HTRA1 can cause severe CARASIL symptoms.

Genetic screening for NUDT15 polymorphisms is crucial for patients taking azathioprine, especially in Asians.

Autism's genetics are linked with early age of puberty and less hair loss, but not with hormone levels or polycystic ovary syndrome.

Early hormones shape sex-specific differences in rat glands.

A genetic mutation in the DCAF17 gene caused Woodhouse-Sakati syndrome in a Chinese patient from a related family.

A 9-year-old Hispanic girl has Uncombable Hair Syndrome, which may improve with age and biotin treatment.

Rheumatology clinics should always provide preconception counseling for women on DMARDs.

Three specific genetic variants cause severe skin issues in children with EBS, highlighting the need for early genetic screening.

Oral tofacitinib may be an effective future treatment for children with severe alopecia areata, but more research is needed.

A girl with a rare genetic condition affecting hair and nails also developed a common type of hair loss, suggesting a possible genetic link.

Removing one ovary helped treat a woman's severe PCOS symptoms when medicine didn't work.

Sodium valproate caused vomiting, hair loss, loss of appetite, abdominal pain, weight gain, and anemia in young children with epilepsy.

Acne can appear or persist in adulthood due to hormonal changes, external factors, or substance use, and requires appropriate treatment.

A child with Olmsted syndrome showed mild improvement in hair and skin issues with treatment.

Maternal aspartame consumption during pregnancy leads to skin damage and higher apoptosis in newborn rat offspring.

A girl lost her hair due to being given the wrong medication because of a pharmacy's computer error.