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Sonidegib and vismodegib are similarly effective for advanced basal cell carcinoma, but sonidegib might have a slightly better safety profile.

A new gene mutation is linked to monilethrix in the studied family.

The flaky skin mouse mutation is a natural model for studying human psoriasis.

A mutation in the hHb3 gene is linked to the hair disorder monilethrix.

A new classification for trichothiodystrophy helps identify genetic causes and potential treatments.

Finasteride use is linked to a lower risk of bladder cancer, especially in Caucasians and Hispanics.

Common variants in the Trichohyalin gene are linked to straight hair in Europeans.

"Bider" markings in Dun Mongolian horses are caused by a complex network of genes and pathways.

A new genetic mutation was found causing hair and eye issues in a boy.

Mutations in the DSG4 gene cause specific hair and scalp issues.

The KRTAP36-2 gene in sheep affects wool yield.

The document concludes that detailed clinical descriptions of seven family cases help understand dominant dystrophic epidermolysis bullosa's symptoms and inheritance.

Different harmful mutations in the CDH3 gene cause HJMD, but symptoms vary among individuals.

A deletion in the CDH3 gene causes a rare disorder with short hair and vision loss.

The patient with a misplaced pituitary gland and interrupted pituitary stalk is being treated with hormone replacement.

A patient with a new PLEC gene mutation showed symptoms of both muscular dystrophy and myasthenia gravis, which improved with steroid treatment.

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I cannot provide a summary without content from the document.

Both laser treatments improved acne scars similarly, but the Nd:YAG laser was safer and less painful, while the Er:YAG laser left patients slightly more satisfied.

A genetic variant in the KRT25 gene causes tightly curled hair.

Becker's Nevus Syndrome is a rare condition with a skin patch and possible bone and muscle abnormalities, treated mainly for appearance.

Dysplastic nevi have unique gene expressions, making them distinct from common melanocytic nevi.

Variant G of the KRTAP20-1 gene improves wool curliness in Chinese Tan sheep.

Deleting the MAD2L1 gene in mice led to rapid tumor growth despite chromosomal instability.

A new mutation in the ST14 gene was found in a patient with ARIH syndrome, showing milder symptoms and no tooth issues.

Oleosomes help cell growth in Sesbania rostrata nodules but don't aid nitrogen fixation.

Sika deer shoulder hair is good for analysis.

The report expanded knowledge of MBTPS1-related disorders by identifying new symptoms.