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Azathioprine's effectiveness and safety require careful monitoring and more research, especially regarding its use with corticosteroids and the role of TPMT status in patients.

No link between scalp patterns and alopecia severity in children, but more severe cases often had nail abnormalities.

Alopecia Areata has no cure, treatments are limited, and the condition often recurs, but new therapies like JAK inhibitors show promise.

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

Most HIV patients develop skin symptoms that can indicate the stage of their disease.

Trichoscopy is reliable for diagnosing Temporal Triangular Alopecia and can prevent unnecessary biopsies and wrong treatments.

Congenital triangular alopecia is a hair loss condition present from birth or early childhood with no effective treatment needed.

Removing a testicular tumor in a dog reduced its aggressive behavior and skin problems.

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

Combining PRP and laser treatments improves hair density best for androgenetic alopecia.

A Brazilian male with IFAP syndrome has a unique genetic variant causing his condition.

Rapamycin reduces skin cell growth and tumor development by affecting cell signaling in mice.

Congenital triangular alopecia and vitiligo can occur together, but treatment for one may not affect the other.

Non-motor symptoms in myasthenia gravis are common and need early diagnosis for better management.

Myasthenia gravis can affect both motor and non-motor systems due to immune system issues.

A patient with Ivemark syndrome developed mixed type vitiligo after a hepatitis C infection, showing different treatment responses and immune cell involvement in the skin.

The document concludes that better targeted treatments are needed for wound healing, and single-cell technologies may improve cell-based therapies.

A 12-year-old girl was misdiagnosed with alopecia areata but actually had a nevus sebaceus with a genetic mutation.

Active oxygen species might be involved in skin tumor growth, but their exact role is unclear.

MendelVar is a tool that helps identify important genes by combining GWAS data with Mendelian disease information.

Using a method of stretching skin multiple times can help cover large bald spots on the scalp, but it takes a long time and isn't good for kids.

A patient with a rare disease had a unique genetic mutation linked to their symptoms.

Zinc pyrithione needs targeted delivery to the scalp for effective dandruff treatment.

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

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

A 23-year-old woman's missed periods were caused by a rare genetic disorder treated with hormone patches.

Hair diseases can have psychological effects and should be treated with a combination of psychosomatic care, therapy, and medication.

The study concluded that hair loss in Indian women is not significantly linked to anemia or thyroid problems, but checking thyroid function could help those with ongoing hair loss.

Herpes gestationis is linked to certain antigens, atopic eczema affects T cell populations and may be eased by breastfeeding, higher doses of anti-androgen treatment can improve androgenic alopecia, topical minoxidil increases hair thickness, long-term methotrexate therapy can cause liver fibrosis in psoriasis patients, and Lichen Sclerosus et Atrophicus patients aren't at higher risk for autoimmune disorders.

Temporal triangular alopecia is a non-scarring hair loss in children, often linked to other health conditions.