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Stopping methotrexate might reverse lymphoma-like conditions in some patients.

A woman with subacute cutaneous lupus erythematosus had widespread skin symptoms triggered by medication and sunlight, which improved with specific treatments.

A man with a rare skin condition and a new gene mutation developed high calcium levels due to his treatment.

Genetic testing for EGFR mutations is crucial in similar cases.

A woman with HIV had a severe skin condition that improved with antiretroviral therapy.

A child with trichothiodystrophy also had autoimmune thyroiditis and anemia, which is a new finding.

Controlling Tslp can improve health in AEC syndrome patients.

Fish oil improves skin health in people with diabetes and high cholesterol.

An American Bully with a genetic skin condition improved significantly with specific topical treatments.

Some patients with mycosis fungoides or Sézary syndrome experience hair loss, which may be similar to alopecia areata or linked to skin lesions, possibly due to abnormal T cells, and bexarotene can help treat it.

Artemis protein may help control hair growth and health by influencing cell processes.

Understanding skin structure and development helps diagnose and treat skin disorders.

Different sPLA2 enzymes affect immunity, skin and hair health, reproduction, and may be potential targets for therapy.

The document concludes that early diagnosis and a comprehensive treatment plan are crucial for managing hair loss in children, with a focus on both medical and psychological support.

The document concludes that hair loss is common and can be treated with medications like minoxidil or surgical options, and it significantly affects people's psychological well-being.

Toxic Shock Syndrome mainly affects menstruating women, can recur, and is linked to staph bacteria, with rapid treatment being crucial.

Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

Rare changes in the KRT82 gene are linked to a higher risk of Alopecia Areata.

A woman had a rare reaction to ear piercing that caused earlobe swelling, which was best treated by removing the piercing and not re-piercing.

New treatments targeting specific genes show promise for treating keratin disorders.

Environmental factors can cause mutations in skin proteins, leading to skin disorders.

Mutations in specific keratin genes cause improper hair structure in mice due to faulty keratin protein assembly.

Brodalumab effectively treated a man's severe hand and foot psoriasis.

The document reports the first Brazilian case of a girl with Becker nevus syndrome, characterized by skin changes, breast underdevelopment, and scoliosis.

Combining minoxidil and plant extracts improved hair growth in a boy with a rare genetic disorder.

An 8-year-old girl with vitiligo developed extra hair growth on her knee after using tacrolimus ointment.

Trichoscopy is a useful tool for diagnosing hair disorders without pulling out hair.

Hair follicle-derived IL-7 and IL-15 are crucial for maintaining skin-resident memory T cells and could be targeted for treating skin diseases and lymphoma.

A 3-year-old boy lost all his hair due to a rare reaction to phenobarbital, but it grew back after steroid treatment.

Methotrexate caused a rare skin rash in a rheumatoid arthritis patient, which resolved after stopping the drug.