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Immunosuppressive and anti-TNF therapies in IBD patients can increase the risk of skin cancer and cause various skin issues.

A girl with Becker naevus syndrome has a genetic variant in the ACTB gene related to her symptoms.

Prenatal genetic diagnosis may not predict MELAS syndrome severity in offspring.

A rare case of Cushing's syndrome and pheochromocytoma requires careful re-evaluation to avoid complications.

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

Metreleptin treatment significantly improved metabolic health in a boy with congenital generalized lipodystrophy.

Fragile hair in children is rarely linked to trichothiodystrophy (TTD).

Two patients treated with TAC for mouth fibrosis improved but developed Cushing's Syndrome symptoms.

People with PCNT mutations often develop severe insulin resistance and early-onset diabetes during childhood or adolescence.

The LMNA mutation affects skin structure even in asymptomatic carriers.

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

Human dermal fibroblasts are the main cells targeted by a virus that can cause a deadly skin cancer, and a certain inhibitor can effectively block this infection.

Deleting TNFα gene reduces skin cancer risk in certain mice.

Trametinib can cause skin issues, but they can often be managed without stopping the drug.

Mesenchymal stem cells may effectively treat and prevent allergic skin conditions.

Cronkhite-Canada syndrome causes chronic diarrhea and has a poor prognosis despite treatment.

Genetic mutation and carcinogen treatment are both needed for skin cancer to develop in these specific mice.

Lack of cystatin M/E causes thin hair and dry skin.

One cat with low thyroid hormone had growth issues, and another with high thyroid hormone had skin problems; both got better with treatment.

Folliculotropic mycosis fungoides has unique molecular features and cell interactions that could guide targeted therapy.

Teprotumumab for thyroid eye disease commonly causes fatigue, brittle nails, dry eyes, hair loss, muscle spasms, and dry mouth, with rare serious events like blood clots.

A specific gene change plus an additional mutation in the same gene cause hereditary trichilemmal cysts.

A rare genetic disorder causes sparse hair and vision loss due to a CDH3 gene mutation.

Cronkhite-Canada syndrome can cause multiple gastrointestinal polyps and various physical symptoms.

A young woman with a rare skin cancer was diagnosed late because her symptoms were unusual for the disease.

Some treatments like methotrexate with prednisone might help juvenile morphea, but more research is needed to confirm.

New therapies and trials are needed for Merkel cell carcinoma, a tough skin cancer.

A Laotian man with unusual skin changes and multiple growths in his gut was diagnosed with Cronkhite-Canada Syndrome and improved with nutritional and immune-based treatments.

People with myotonic dystrophy type 1 tend to develop basal cell carcinoma at a younger age but not more frequently than others.

New guidelines stress early diagnosis and lifestyle changes to manage metabolic syndrome and prevent complications.