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Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

Fractional infrared technology is effective and safe for treating cervical laxity.

Keratin fibers in hair twist left-handed.

Faulty LEF1 activation causes faster skin cell differentiation in premature aging syndrome.

Rothmund-Thomson syndrome causes skin changes, hair loss, and slightly high lysine and cystine in urine.

Early detection and treatment are crucial to prevent irreversible hair loss in Lichen Planopilaris.

The patient with EEC syndrome had scarring alopecia due to deep folliculitis, possibly linked to abnormal hair structure.

Hair restoration surgery can cause muscle and joint problems due to poor workplace setup.

Ulcerative sarcoidosis in body folds is rare and improved with prednisone and hydroxychloroquine.

This method effectively reconstructs scarred penopubic junctions after surgery.

A new type of pachyonychia congenita may exist, caused by a different keratin mutation.

Two Hispanic women developed Plica neuropathica, a condition causing tangled hair, possibly due to hair damage and various risk factors.

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

Early diagnosis and a multidisciplinary approach are crucial for children with Trichothiodystrophy and hidden learning disorders.

Three siblings had both Vohwinkel's disease and congenital alopecia, with no effective treatment.

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

A hereditary condition causes hair loss and twisted hair in some family members.

A 6-year-old boy's leg hair loss was due to friction from sitting cross-legged, and it usually resolves on its own.

Age-related hair curvature increases due to internal structural changes from grooming.

Researchers found a new mutation in the FERMT1 gene in a Spanish family with Kindler syndrome.

Mutations in the ACTB gene cause Becker’s nevi and may lead to muscle issues in Becker’s nevus syndrome.

A specific gene mutation causes Olmsted syndrome.

Trichoscopy can reveal specific hair and scalp changes in linear morphea.

A 34-year-old woman had itchy black bumps on her face due to a condition called trichostasis spinulosa.

A 5-year-old girl with a rare skin disorder was effectively treated with skin creams instead of oral medication.

Palmaris longus muscle absence is uncommon and not linked to gender, hand side, or finger ratio.

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

Costovertebral arthritis can cause chronic back pain in SLE patients and needs thorough evaluation.