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A new severe form of monilethrix syndrome includes hair loss, scalp itching, cataracts, and distinct facial features.

A new genetic mutation was found causing hair and eye issues in a boy.

Unani medicine may help treat a rare, hard-to-treat hair loss pattern in children.

Snakes and worm lizards lost claw proteins due to similar evolutionary changes.

Atrichia with papular lesions causes irreversible hair loss from infancy and is often misdiagnosed.

Trichilemmal cysts can appear on children's eyelids and may be mistaken for other conditions.

A young boy with a rare skin and nail condition improved significantly with simple topical treatments.

Netherton's disease causes multiple hair defects.

Hand-foot-mouth disease may cause nail loss in children.

Lhx2 helps retinal cells respond to signals for eye development.

A rare genetic deletion in the KRT1 gene causes unique skin symptoms in a family.

Hair plucking quickly increases antizyme, reducing a specific enzyme activity in rats.

A man had four testicles, two of which were outside the scrotum and looked like fatty lumps.

Mouse amnion can turn into skin and hair follicles with help from certain cells and factors.

Epidermolytic ichthyosis can be inherited in a semidominant way with mild symptoms in carriers.

Mutations in the SHH pathway in certain skin cells can cause skin tumors and abnormal hair growth.

Two siblings had a rare immune disorder caused by a FOXN1 gene mutation.

A rare skin condition caused droopy and outward-turning eyelids in a patient.

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

One twin girl has Loose anagen syndrome with poorly anchored hair, diagnosed with a simple hair pull test, while her identical twin does not have the condition.

A 2-year-old boy with a rare brain malformation may have Gomez–López-Hernández syndrome.

A baby with a skin condition improved with treatment but developed a rare form of the condition affecting only his trunk.

A specific gene mutation causes hair loss and potential eye issues, even if vision seems normal.

Mutations in the AP1B1 gene cause a new syndrome with skin, hearing, and developmental issues.

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

A 17-year-old girl and her brothers have a rare hair condition with long eyelashes, thick eyebrows, and easily pluckable hair.

A 15-year-old girl has a skin condition causing blisters on her feet, likely inherited from her family.

A 4-year-old girl has a rare condition causing hairlessness and skin bumps, but normal teeth and sweating.

A man had rare skin tumors with bone formation and cholesterol deposits.