Search

everythingexperts & clinicslearnresearchcommunity

for

Search:↓

Trichohyalin is a versatile protein involved in hair and skin structure.

Recognizing ultrastructures of cashmere goat hair follicles helps identify and locate follicle layers.

The mummified girl likely died from undernourishment and illness.

Early biopsy is crucial for diagnosing rare skin sarcoidosis, improving treatment.

Hair structural proteins are synthesized sequentially in specific cells, offering a new way to study hair proteins and defects.

A person had two different benign skin tumors, a trichoadenoma and melanocytic naevi, at the same time but in different places on the face.

Two boys developed a viral skin infection during chemotherapy, which resolved with improved immune function.

Fibroblasts can be mistaken for neural cells, so functional validation is needed.

NISCH syndrome is a rare genetic disorder affecting skin and liver, with variable symptoms and limited treatment options.

Copper treatments increase copper in all tissues, but brindled female mice accumulate much more copper in their kidneys without clinical effects, unlike brindled male mice where brain copper deficiency is clinically significant.

The study found that hair fragility in Pili annulati may be caused by cavities and damage within the hair shafts.

A 78-year-old man with Cronkhite-Canada syndrome improved significantly after treatment and remains symptom-free.

Chemotherapy caused the patient's hair to have alternating thick and thin segments.

Melanocytes can regenerate around hair follicles in bullous pemphigoid, especially in patients with darker skin.

Accurate diagnosis of granular parakeratosis is crucial for effective treatment and improvement.

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

Friedreich's ataxia causes thin, weak hair with surface damage and cavities.

Porokeratotic eccrine and hair follicle nevus is a very rare skin disorder possibly caused by a GJB2 gene mutation.

Hair casts, also called pseudonits, are often mistaken for other conditions.

A 12-year-old boy in rural south India had a rare skin condition causing hair loss and inability to sweat.

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

Trichocytic differentiation starts in cells with epithelial cytokeratins, transitioning to trichocytic cytokeratins in hair and gradually in nails.

An 8-year-old girl has a rare, irreversible hair loss condition caused by a genetic mutation.

Two dogs in Korea were diagnosed with a rare skin condition usually seen in cats.

The man's hair loss and skin papules were diagnosed as atrichia with papular lesions, not alopecia areata universalis.

Arginine converts to citrulline in hair follicles as proteins harden.

Buschke-Ollendorff syndrome is a rare genetic disorder causing skin and bone changes, with some cases also showing ADHD or developmental delays.

A new gene variant in a girl with Coffin-Lowry Syndrome may link the condition to early puberty.

The protein FLCN is involved in cellular cleanup and is regulated by ULK1.

An 8-year-old girl had a rare, benign skin tumor on her forehead.