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

Jawless vertebrates have teeth proteins similar to those in mammalian hair and nails.

A new mutation in the hHb1 keratin gene is linked to the hair disorder monilethrix.

Mutations in specific genes cause different types of ectodermal dysplasias.

THH and PAD type III appear together early in hair growth, but deiminated THH appears later, suggesting another factor is involved.

Loss of Msx2 function causes eye development issues similar to Peters anomaly.

A 10-year-old boy with abnormal genital development had surgery and tests to find the cause and plan treatment.

Blocking hair follicle development stops key gene signals needed for hair growth in mice.

A man with alopecia universalis regrew hair temporarily after a bone treatment.

Researchers found a new genetic mutation causing a rare hair loss condition in the first Japanese child studied.

The woman has a rare skin condition called follicular Dowling-Degos disease, which has limited treatment options.

Patients treated with long-term intralesional corticosteroids for alopecia areata should be monitored for bone density changes and advised on osteoporosis prevention.

Two rare bald spots on the back of the scalp were found to be lupus, not alopecia areata.

Early diagnosis and treatment of congenital adrenal hyperplasia are crucial to manage symptoms and prevent complications.

A patient developed excess hair and skin issues on the same side after wearing a cast.

A child has a rare hair and skin disorder due to specific gene variants, suggesting broader genetic testing is needed.

Truncating mutations in the C2orf37 gene cause Woodhouse–Sakati syndrome.

A family showed a new condition with inherited hair loss and skin changes, possibly due to one genetic disorder.

Custom-designed implants effectively repaired skull damage in most soldiers injured in combat.

Frontal hair in male pattern baldness shows reduced growth and thickness.

Foxi3 expression in developing teeth and hair is controlled by the ectodysplasin pathway.

A mother and daughter have a rare genetic hair loss disorder with no effective treatment.

A specific gene mutation causes varying hair loss severity in a Pakistani family.

Monilethrix is a genetic hair disorder affecting hair shape, seen in two brothers.

Onychomatricoma is a unique nail tumor, not related to other hair-related tumors.

Early diagnosis and multidisciplinary care, including orthopedic surgery, can prevent long-term disability in IFAP syndrome.

Certain nail conditions can suggest thyroid problems, with different symptoms for underactive (slow, thin nails) and overactive (spoon-shaped, brittle nails) thyroid.

A boy's skin fragility and sparse hair were caused by a genetic mutation affecting skin cell adhesion.

Toy poodles may develop harmless mineral deposits around hair follicles as they age.

Mice with human-like EGFR had growth issues, skin defects, heart problems, and unusual bone development.