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Carriers of a specific gene mutation have subtle skin changes without visible symptoms.

Erythema nodosum linked to kerion can be treated effectively with antifungals and steroids to reduce scarring.

The p.P25L mutation in the KRT5 gene causes a rare skin condition that worsens over time and may lead to hair loss starting in young adulthood.

Dermoscopy is useful for diagnosing Atrichia with Papular Lesions in children without needing a biopsy.

A boy with Pachyonychia congenita has a confirmed gene mutation, highlighting the need for a local genetic database in India.

Recognizing keratosis pilaris in all skin tones helps diagnose related skin issues and reduce distress.

A patient with a skin condition had unusual scarring hair loss but improved with treatment.

Trichorhinophalangeal syndrome causes hair, facial, and bone issues, with no specific treatment beyond gentle care.

A girl with a rare skin condition improved after one month of treatment with acitretin.

Four new cases confirmed the unique features of follicular porokeratosis.

Dermatologists should consider congenital syndromes like TRPS in young adults with early hair loss.

A 10-year-old boy recovered from a scalp infection caused by a fungus after treatment with itraconazole.

A 69-year-old woman has a fast-growing hand lesion that didn't improve with salicylic acid.

Treatment with vitamin A did not improve the child's skin condition.

An elderly man's non-healing scalp lesion was successfully treated with a strong topical steroid.

The term "porokeratotic adnexal ostial nevus" is proposed to unify overlapping skin conditions involving eccrine and hair follicles.

A new pair of mouse keratins, 65 kD and 48 kD, are found in specific skin areas and are linked to a unique skin differentiation type.

LEKTI is crucial for skin barrier and immune function, affecting conditions like Netherton syndrome and atopic dermatitis.

The cyst had unusual keratin spherules and resembled bone marrow.

The newborn's skin blistering is due to a genetic condition called epidermolytic hyperkeratosis.

Autoimmune myopathy may be linked to hair loss and skin depigmentation.

Recognizing scalp symptoms in PRP is crucial for proper diagnosis and treatment.

Trichostasis spinulosa can look like acne but usually affects adults, not children.

Certain genetic changes in the LSS gene cause a rare skin and hair condition.

A rare skin condition was confirmed to be associated with a specific virus in a young girl.