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A rare case shows a possible link between Neurofibromatosis type 1 and Becker nevus due to genetic mutations.

A man with scalp and neck skin issues improved after a year of oral isotretinoin.

Keratin 17 gene mutations cause both steatocystoma multiplex and pachyonychia congenita type 2.

Zinc supplements improved the girl's skin and hair condition.

Melanocyte stem cells can become melanoma, resembling human melanoma.

A 37-year-old male with severe skin and internal issues has a rare inherited skin condition called dystrophic epidermolysis bullosa.

A 15-year-old with KID syndrome developed a rare skin condition called PEHFN.

Scalp pemphigus vulgaris can be effectively treated with low-dose prednisone and triamcinolone.

The horse had a rare type of hair loss caused by immune cells attacking hair follicles.

The new protocol using Cellutome™ and RCM safely assesses wound healing in detail.

Skin can produce blood cells, often due to disease, which might lead to new treatments for skin and blood conditions.

An infant developed excessive hair growth after a bone marrow transplant and cyclosporine treatment.

Vitamin B12 deficiency can cause reversible skin darkening.

A 25-year-old man with multiple skin tumors was successfully treated with acitretin and methotrexate.

A 50-year-old woman with breast cancer developed an autoimmune skin disorder, highlighting the need for thorough checks and team-based treatment.

A 66-year-old woman with skin lesions and other symptoms improved after treatment for porphyria cutanea tarda.

BAP1 mutations are rare in pediatric melanocytic tumors and may develop later in life.

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

Pachyonychia congenita is linked to a keratin gene on chromosome 17.

Different types of stem cells in the skin contribute to the variety of melanoma forms.

MMP-19 may worsen skin diseases by affecting skin growth and inflammation.

Mini punch grafts effectively healed a large ulcer in a child.

Pseudopelade is likely an independent disease due to its distinct features.

Mesothelioma of the tunica vaginalis testis is rare, often high-grade, and has a median survival of about 24 months.

Necrobiosis lipoidica may need new criteria for accurate diagnosis due to similarities with another condition.

Narrowband UVB therapy significantly improved a child's rare skin condition.

Focal palmoplantar callosities may help diagnose non-Herlitz junctional epidermolysis bullosa.

Microneedling for hair loss may cause skin cancer.

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

An 11-year-old Greek girl was diagnosed with a rare genetic disorder, highlighting the importance of genetic testing and family history.