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Microstimulation of certain facial and mouth nerves can evoke specific sensations, while deeper nerves may require multiple stimulations to affect perception.

cDermo-1 causes dense skin, feathers, and scales in chickens.

A new gene mutation causes a rare type of hair loss.

A 5-year-old girl with a rare genetic disorder, lipoid proteinosis, showed reduced new lesions but persistent scars after avoiding skin trauma.

Mutant Cx43 causes slower wound healing and hair growth issues in ODDD.

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

Mutations in the HOXC13 gene cause hair and nail development issues.

Mice without certain skin proteins had abnormal skin and hair development.

A painless cheek lump was misdiagnosed but later identified as a rare benign skin lesion called pilomatrixoma.

Accurate diagnosis of APL is crucial to avoid unnecessary treatments.

Juvenile dermatomyositis can worsen quickly and needs strong treatment.

A mutation in the EDNRA gene causes Oro-Oto-Cardiac syndrome, affecting face and heart development.

Desmosomes are crucial for skin and heart development, and JNK may help regulate them.

Too much Smad7 can cause serious changes in skin tissues, including problems with hair growth, thymus shrinkage, and eye development issues.

An 11-year-old boy in Saudi Arabia has a rare case of hypoparathyroidism with severe brain calcifications but normal development and no known cause.

Mutations in specific genes cause certain congenital defects in dogs, aiding in understanding similar human diseases.

Netherton's disease causes multiple hair defects.

Hair follicle cells can help regenerate teeth.

Canine circumanal glands develop from hair follicle sheath cells, not sebaceous glands, and lack exocrine ducts.

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

The name Janus is fitting for JAK inhibitors as they revolutionize dermatology treatments.

A 4-year-old girl had a rare hair disorder affecting only part of her scalp.

Oral JAK inhibitors are safe for alopecia areata, but baricitinib may cause more acne and infections.

Tissue-engineered skin substitutes can model junctional epidermolysis bullosa and may help develop gene therapy.

Upadacitinib significantly improved a man's severe scalp condition when other treatments failed.

Endoscopy-assisted surgery for craniosynostosis showed excellent outcomes with minimal complications and most patients went home the day after surgery.

Gap junctions help control feather pattern formation in chickens.

A woman's hair grew back with baricitinib treatment, but she developed a temporary hairy tongue that was treated with regular tongue brushing.

Temporal triangular alopecia usually starts in early childhood and treatment with Minoxidil has limited effectiveness.