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A new gene mutation causes vitamin D resistance and rickets, treatable with calcium therapy.

Four children had unmanageable pale blond hair due to uncombable-hair syndrome.

Patients with renal disease may develop vitamin A toxicity even with low-dose supplements.

Zinc therapy improved hair health in a girl with acrodermatitis enteropathica.

Parathyroid adenoma can cause hyperparathyroidism and hair loss in children.

A 7-year-old girl experienced temporary hair loss due to radiation, with signs of possible hair regrowth.

Genetic testing confirmed a rare skin disorder in a young girl, which improved with zinc supplementation.

A TP63 gene mutation causes significant hair loss and mild skin, nail, and tooth abnormalities.

The study concluded that PKP1 is essential for skin integrity and hair growth, and its dysfunction causes the symptoms of ectodermal dysplasia/skin fragility syndrome.

Norfolk Terriers have a genetic skin defect causing scaling and blisters due to a keratin issue.

The man has a genetic skin condition called pachyonychia congenita.

Hair malformations may occur due to timing issues in hair development.

A gene deletion in mice causes weak protein, immune issues, hair loss, airway problems, and wasting disease.

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

Too much vitamin A can cause serious health problems.

The study found that pili bifurcati causes hair to intermittently split into two branches, each with its own outer layer.

A baby with KID syndrome died from infections and organ failure at 18 months old.

Long-term use of seizure medications can disrupt calcium metabolism, but this can be treated with vitamin D or UV light and does not affect seizure control.

The treatment improved facial structure and corrected bite issues in patients.

The study found that hair fragility in Pili annulati may be caused by cavities and damage within the hair shafts.

Congenital atrichia with papular lesions is often misdiagnosed, and new diagnostic criteria can improve accuracy.

THA is a rare condition with no significant clinical consequences if thyroid function is normal.

People with hypohidrotic ectodermal dysplasia are more likely to experience long-term fatigue and hair loss after COVID-19.

Monilethrix is not caused by a metabolic defect.

A specific gene mutation causes vitamin D-resistant rickets and hair loss.

A rare gene variant causes hair and nail issues in a family.

The LMNA mutation affects skin structure even in asymptomatic carriers.

White-tailed deer can get a hair loss condition that might make them more vulnerable to environmental threats.

Vitamin D Dependent Rickets Type-2A can cause complete hair loss and bone growth issues in infants.

A boy with Oculodentodigital syndrome had a unique GJA1 gene mutation causing his symptoms.