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The combined treatment effectively managed severe skin issues in Olmsted syndrome.

Nagashima-type palmoplantar keratosis in Asians is caused by a SERPINB7 gene mutation.

Certain genetic changes in the LSS gene cause a rare skin and hair condition.

People with Birt-Hogg-Dubé syndrome often have lung problems and delayed diagnosis, and better recognition of CT scan signs could improve diagnosis and management.

Ichthyosis with confetti is a genetic skin disorder with consistent ectodermal malformations and various KRT10 gene mutations.

A 6-year-old girl was diagnosed with a rare hair disorder and started treatment with topical minoxidil.

A woman with a unique syndrome similar to TRPS has a genetic change near the TRPS1 gene, affecting its regulation.

The UK's EDS National Diagnostic Service found that early diagnosis, lifestyle advice, and regular check-ups are crucial for managing vascular Ehlers-Danlos syndrome. A combination of losartan and bisoprolol can reduce vascular events, improving survival and quality of life.

A patient with Myotonic dystrophy type 1 had multiple tongue hemangiomas and was sensitive to anesthesia.

Some people with schwannomatosis have a new type of mutation in the LZTR1 gene.

Early and aggressive treatment is crucial for preserving vision in infants with AEC syndrome.

Scientists used stem cells to create a model of the skin disease Epidermolysis Bullosa simplex, which helped them understand its molecular mechanisms and could aid in finding treatments.

CCCA can affect both genders and all ages, and it has a genetic component.

Monilethrix is a rare, inherited condition causing fragile hair and hair loss, with no cure but some treatments may help.

A girl with excessive hair growth had a genetic change on chromosome 17 that reduced the activity of two genes linked to hair growth.

A new mutation in the Connexin 26 gene was found in a patient with KID syndrome, expanding the known disorders linked to this gene.

The protein FLCN is involved in cellular cleanup and is regulated by ULK1.

Rapp-Hodgkin syndrome, AEC, and EEC are different expressions of the same genetic disorder caused by TP63 gene mutations.

The document suggests a possible link between FAM111B gene mutations and increased cancer risk, particularly pancreatic cancer.

Dermoscopy quickly and accurately diagnosed a rare hair disorder in a 12-year-old girl.

Substance P may play a role in the inflammation seen in keratosis follicularis spinulosa decalvans.

PRP with microneedling improves hair growth and patient satisfaction more than injections for androgenetic alopecia.

A man with myotonic dystrophy type 1 had 28 skin cancers, suggesting a link between the disease and skin cancer, emphasizing the need for sun protection and regular skin checks.

Dermoscopy helped diagnose a rare hair disorder in a 2-year-old boy.

A TP63 gene mutation causes significant hair loss and mild skin, nail, and tooth abnormalities.

Exosome treatment safely increases hair density in male patients with androgenetic alopecia.

A 23-year-old Syrian woman has two rare hair disorders, and avoiding hair treatments plus using vitamins and minoxidil may help.

Certain genetic mutations can lower bad cholesterol and reduce heart disease risk, leading to effective cholesterol-lowering drugs.

Minoxidil improved hair growth in a child with a rare genetic disorder.