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A woman and her daughter had thallium poisoning from a herbal drink and rodenticide, causing hair loss and other symptoms.

Dermoscopy helped diagnose a rare hair disorder in a 2-year-old boy.

Alopecia in patients with epidermolysis bullosa varies in severity and is often caused by skin blistering or trauma.

The document concludes that certain rats and mice are useful for studying hair loss in humans and testing treatments.

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

A baby was diagnosed with IFAP syndrome due to a new genetic mutation, showing severe skin and developmental issues.

Mutations in the KLHL24 gene cause a skin disorder in some Russian families.

The combination therapy of PEG-IFN α-2a and Ribavirin can cause widespread hair loss and skin reactions.

Contaminated wheat caused hair loss and other symptoms due to high selenium, but washing it with alkaline water helped.

A Jordanian family with Clouston syndrome has a common GJB6 gene mutation.

A Chinese male with a new genetic mutation has a skin condition and severe urinary issues, with treatments having mixed success.

Targeted therapy with Ustekinumab significantly improved a skin condition called ILVEN, which is caused by mutations in the CARD14 gene.

A 5-year-old boy's skin condition improved with systemic valganciclovir after a cardiac transplant and immunosuppressive therapy.

Skin doctors should recognize and treat conditions like hair-pulling and skin-picking early, often using therapy and medication, to help 50-70% of patients.

SLE patients experience hair loss similar to telogen effluvium, with hair damage and immune activity at hair follicles.

Zinc supplements can resolve skin issues caused by zinc deficiency.

The study found that males with KFSD had severe skin and eye symptoms, while female carriers had milder symptoms.

Most hospitalized children with skin issues were boys, with allergic skin diseases like atopic dermatitis being most common, and treatments were usually topical.

Trichothiodystrophy can be linked to urologic issues and high calcium in urine.

Pincer nails are rare in lupus patients and may be managed conservatively.

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

Platelet-rich plasma treatment significantly increased hair regrowth and decreased discomfort in alopecia patients, making it a potentially better and safer treatment option.

Lupus can affect the scalp and nails, often causing hair loss and nail damage, and needs early aggressive treatment to prevent permanent damage.

Skin problems can be caused or worsened by physical forces and pressure on the skin.

Alopecia areata is an unpredictable autoimmune hair loss condition, treated based on severity, with half of patients regrowing hair within a year without treatment.

JAK inhibitors show promise in effectively treating hair loss from alopecia areata.

Vitamin A toxicity can cause severe health issues and may require a liver transplant if other treatments fail.

A rare genetic mutation found in an Indian family can be detected through prenatal screening.

DPR can show different hair characteristics, as seen in two brothers with normal hair.

Dermatopathia pigmentosa reticularis causes skin discoloration, hair loss, and nail problems.