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Advanced dermoscopy techniques improve diagnosis and treatment monitoring for Kerion celsi but don't guarantee full hair regrowth.

The enzyme DHHC13 is essential for healthy hair and skin, and its deficiency leads to hair loss and skin problems.

High ODC and low K1 and K10 may indicate early skin tumors in mice.

Keratoacanthoma comes from hair follicle cells.

Involucrin is a useful marker for keratinocyte differentiation in mice.

An 8-year-old girl has a rare genetic disorder causing complete, irreversible hair loss and skin bumps.

Malassezia in cat skin biopsies may indicate internal cancer.

A rare skin condition usually on the face was found on a man's heel.

A simple classification based on symptoms helps diagnose and treat inherited skin disorders in Japan.

A man in his 30s had patchy hair loss on his leg due to primary follicular mucinosis.

Nilotinib can cause generalized keratosis pilaris.

Two new types of eyelid cysts were identified, each with different treatment challenges.

Onychomatricoma is a unique nail tumor that mimics the entire nail unit and is not related to other hair-related tumors.

Keratoacanthoma is a common, usually non-dangerous skin tumor that looks like squamous cell carcinoma but rarely becomes severe.

Topical 6% salicylic acid effectively reduced skin plaques in a patient with wooly hair and palmoplantar keratoderma.

Cathepsin E is crucial for normal skin cell differentiation and development.

Keratin 15 is not a reliable sole marker for identifying epidermal stem cells because it's found in various cell types.

Accurate diagnosis of EFFC is crucial for effective counseling and cosmetic care.

Nevus sebaceous is identified by unique skin changes, including thickened skin, fewer hair follicles, and many sebaceous glands.

Keratins K6 and K16 are expressed more freely in regenerating mouse skin than K1 and K10.

The conclusion is that Darier-White disease was accurately described by White but he missed the key feature of dyskeratotic cells which Darier identified.

The patient has a rare skin condition that shows features of two known disorders.

c-Myc activation in mouse skin increases sebaceous gland growth and affects hair follicle development.

Basal cell carcinoma shows keratin patterns similar to undifferentiated hair follicle cells.

A rare, harmless hair condition was found in an infant's eyebrow, needing no treatment.

A rare benign skin growth called melanocytic matricoma was identified in a 69-year-old man.

DPR can show different hair characteristics, as seen in two brothers with normal hair.

Monilethrix is linked to the type II keratin gene on chromosome 12q13.