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A new mutation in the XEDAR gene might cause a rare skin condition called hypohidrotic ectodermal dysplasia.

Zinc deficiency in alcoholic cirrhosis patients causes skin issues, and zinc treatment improves symptoms.

Many people in Misurata City have low vitamin D, especially women and those aged 35-45, with levels dropping in winter and spring.

Genetic testing for EGFR mutations is crucial in similar cases.

Disrupting Acvr1b in mice causes severe hair loss and thicker skin.

The rash on the infant indicated a serious underlying condition.

Early and accurate diagnosis of primary vitreoretinal lymphoma is crucial to prevent serious complications.

The study concluded that low iron and vitamin D levels in women might play a role in chronic hair loss, despite no significant difference between those with and without hair loss.

ATP6AP1‐CDG can cause hearing loss, hair loss, and protein issues, even in female carriers.

Valproic acid treatment may cause temporary hair loss due to reduced zinc and biotinidase levels, which tend to normalize after 6 months.

Trichothiodystrophy causes unusual hair and developmental issues.

Follicular red dots may be a normal feature seen in people with less skin pigmentation, not necessarily indicating a scalp disorder.

Some children with methylmalonic and propionic acidaemias have skin problems related to their condition and diet.

Malabsorption can cause skin issues like pigmentation changes and hair loss, which improve with treatment.

Gorillas in Gabon improved after protein supplements were added to their diet.

People with chronic hair loss often have lower Vitamin B12 levels.

5% topical minoxidil improves hair density and quality in monilethrix patients.

Iron deficiency can cause psychiatric symptoms that improve with proper treatment.

Alopecia areata can show unusual red-dotted vessels and dithranol treatment may mask typical patterns.

Diphencyprone can cause unexpected and possibly permanent vitiligo.

DFMO treatment improves hair growth, muscle tone, and development in Bachmann-Bupp syndrome patients.

Copper deficiency lowers blood and liver copper levels in rats, but not in hair or bones.

Vitiligo patients should be routinely screened for thyroid disease and, if extensive or prolonged, also for RA, PA, and type 2 diabetes.

A specific mutation in the TRPV3 gene causes hair follicle cells to develop improperly, leading to hair loss.

A girl's hair-pulling condition improved greatly after she started vitamin D treatment.

Genetic disorders can disrupt mineral and trace element metabolism, affecting health.

Albumin and prednisone improved symptoms in a woman with Cronkhite-Canada syndrome, revealing potential genetic causes.

FOXN1 gene mutations cause a rare, severe immune disease treatable with cell or tissue transplants.

The young goat had anaplasmosis and copper deficiency.