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Accurate diagnosis and management of rare genian fistulas require combined clinical, radiologic, and histopathologic evaluations.

A new tool allows easier long-term imaging of live skin cells, helping study diseases like skin cancer.

Human hair keratin genes are similar to mouse genes and are specifically expressed in hair follicles.

New genetic mutations linked to rare skin disorders were found in three newborns.

Different keratins have unique expression patterns in mouse skin cells.

Male infertility and genitourinary birth defects are often linked to genetic issues.

The Agouti gene influences pigmentation and may have a developmental role in deer mice.

The mTurq2-Col4a1 mouse model shows how the basement membrane develops in live mammals.

The L412F variant of TLR3 is linked to skin infections, more viral infections, and autoimmune issues.

The peptide IMT-P8 can effectively deliver proteins into the skin and cells for potential skin treatments.

Mutations in the FOXN1 gene cause severe immune issues but don't affect hair and nails.

Certain genetic markers linked to reproductive potential were identified by their impact on a protein's ability to bind to genes.

Fibroblasts can be turned into melanocytes for potential skin treatments.

Gap junctions help control feather pattern formation in chickens.

The STIM1 R304W mutation in mice leads to bone changes and teeth hair growth.

A new mutation in the mitochondrial DNA was found in a boy with MELAS, even though his family didn't show typical signs.

Adding TERT and BMI1 to certain skin cells can improve their ability to create hair follicles in mice.

Hair follicle stem cells use specific chromatin changes to control their growth and differentiation.

The guinea pig α-lactalbumin gene was successfully expressed in the mammary glands of transgenic mice.

Low IRES/Cap translation is linked to higher stem cell potential.

The marker 5-hmC changes in hair follicle stem cells when they start to grow.

Two cases showed skin abnormalities without bone or neural defects.

Monilethrix is a genetic hair disorder affecting hair shape, seen in two brothers.

Researchers created a new mouse model for studying scleroderma.

A rat had a cyst similar to a hair follicle structure.

A new mutation in the FLCN gene linked to Birt-Hogg-Dube syndrome was found, suggesting people with certain lung collapse should be tested for this mutation and screened for kidney and colon cancer.

Accurate diagnosis and early specialist referral are crucial for managing 46,XY Disorders of Sex Development.

Thorough history and examination are crucial for diagnosing genetic disorders like juvenile polyposis and hypomelanosis of Ito.

A specific gene variant causes severe skin issues and increases infection risk, requiring careful medical monitoring.