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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.

People with Myotonic Dystrophy type 1 are more likely to have certain skin conditions, but not more likely to get skin cancer.

New mutations in the DSG4 gene cause a rare hair condition.

The DMI3 gene is essential for nodule development and symbiosis in certain plants.

UTMD with diclofenac and Doxil® improves cancer treatment by boosting immune response and reducing tumor-supporting cells.

Sentinel lymph node biopsy is recommended for all types of desmoplastic melanoma due to higher rates of nodal metastasis.

Sentinel lymph node biopsy is recommended for all types of desmoplastic melanoma due to higher rates of nodal metastasis.

NDP-MSH protects brain cells and reduces inflammation in Parkinson's disease by activating MC1R and involving Tregs.

Myotonic dystrophy should be considered in patients with hair thinning, and genetic counseling is important.

A new CDH3 gene mutation was found in a Spanish patient with sparse hair and eye issues.

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

HtrA2 activity is crucial for normal hair growth by regulating fat cell development.

A specific gene mutation is linked to a hereditary form of dystonia that responds well to certain medications.

A patient with myotonic dystrophy had several autoimmune disorders and thyroid cancer, suggesting a possible link between these conditions.

DNMT1 may help treat hypospadias by improving cell function and preventing unwanted cell changes.

A new genetic mutation in the ODC1 gene causes developmental delay and other symptoms in a young girl.

Metformin/dopamine-derived carbon dots help heal bacteria-infected wounds faster.

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

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

New gene variants linked to a rare inherited hair loss disorder were found in three Chinese families.

Mice lacking steroid 5α-reductase 2 show less aggression and better impulse control.

Two new mutations in the CDH3 gene cause hair loss and vision problems in a young girl.

A new genetic disorder caused by an ODC1 mutation can be treated with DFMO.

A new microneedle system effectively delivers a vasodilator to hair follicles, promoting hair growth better than current treatments.

Baricitinib helped regrow hair in patients with severe alopecia areata after other treatments failed.

Mutations in the DSG4 gene can cause a rare hair disorder similar to monilethrix.

Recognizing minor skin lesions can help identify serious cancer syndromes.

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

Hair root analysis can effectively detect somatic mosaicism in double cortex syndrome.