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Citrullus colocynthis has pain-relieving, anti-inflammatory, antidiabetic, and hair growth benefits, but can cause side effects like colic and diarrhea.

A specific gene mutation in Japanese people can cause varying degrees of hair thinning in adulthood.

Monilethrix is not caused by a metabolic defect.

A child with ectodermal dysplasia-syndactyly syndrome has a new mutation in the NECTIN4 gene.

Rabbits lacking the Hoxc13 gene show similar hair and skin issues to humans with ECTD-9, making them good for research on this condition.

A woman with Castleman's disease died from respiratory failure due to bronchiolitis obliterans.

A new mouse mutation causes skin and hair defects due to a gene change.

A 9-year-old girl has a rare hair disorder causing beaded, sparse hair.

A variant in the KRT31 gene causes a rare hereditary hair disorder called monilethrix.

CaBP1 and 2 are necessary for maintaining calcium currents and hearing in inner ear cells.

Untreated congenital adrenal hyperplasia can lead to complications like stroke and needs glucocorticoid treatment.

Crohn's disease can cause hair loss before other symptoms appear.

Removing the Crif1 gene in mouse skin disrupts skin balance and hair growth.

Cyclosporine can cause a unique skin condition called "cyclosporine-induced folliculodystrophy."

A baby boy with 13q deletion syndrome had eye cancer, a woman's vision improved after stopping a breast cancer drug, a man developed cataracts from using Propecia, and a rare skin disorder called Lipoid Proteinosis was discussed. Also, a tool called OCT is useful for diagnosing macular diseases.

Hair loss in black women needs more research, early intervention, and community education.

A rare case of trichothiodystrophy was found with autism, seizures, and mental retardation.

Eyelash loss can temporarily occur from chemotherapy for retinoblastoma.

A rare genetic disorder causes sparse hair and vision loss due to a CDH3 gene mutation.

A new topical treatment may prevent hair loss from cancer therapy by adjusting cell death processes in hair follicles.

ATP-sensitive potassium channels play a role in chloroquine-induced itch in mice.

Genes linked to fibrosis are more active in people with central centrifugal cicatricial alopecia.

Recurrent NICF is a rare skin condition with unclear causes, involving follicle inflammation and crystal deposits.

Imatinib can cause hair loss due to lichen planopilaris.

CIPK13 and CIPK18 genes are crucial for root hair growth in plants.

Sphynx cats have abnormal hair follicles and keratinization affecting their skin.

CXXC5 can both suppress and promote cancer, making it a complex target for treatment.

A patient with congenital erythropoietic porphyria showed eye issues due to porphyrin buildup.

Cyclosporin A is highly toxic to rats, causing severe health issues and death.