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Pharmacists play a key role in managing the use of anxiety medications and ensuring patients use them correctly.

A specific mutation in the K25 gene causes a rare genetic disorder with curly hair at birth and later hair loss, along with dental issues.

A genetic mutation in the LIPH gene causes tightly curled hair that stops growing in some Japanese individuals.

Minoxidil can improve hair growth in some patients with woolly hair due to LIPH variants, with varying responses and mild side effects.

A gene mutation causes lanceolate hair in rats by disrupting hair shaft integrity.

Nonclassic 21-hydroxylase deficiency is a common, treatable genetic disorder causing reversible symptoms like acne and hair loss.

A patient with Wilson's disease showed hair-pulling behavior as an initial symptom.

Netherton Syndrome is a non-treatable genetic disorder in children causing skin, hair, and allergy issues.

Truncating mutations in the C2orf37 gene cause Woodhouse–Sakati syndrome.

A new mutation in the DCAF17 gene was found to cause Woodhouse-Sakati syndrome in a large family.

Bardet-Biedl syndrome may include under-recognized skin problems related to its metabolic disturbances.

Haplogroup X found in Altaian population supports Amerindian origin.

Two different mutations in the vitamin D receptor gene cause different symptoms and responses to treatment in Lebanese patients with hereditary rickets.

Intravenous calcium therapy is a safe and effective treatment for a rare type of rickets.

The document concludes that individuals with a rare genetic disorder linked to the AEBP1 gene may experience a unique type of hair loss and should be monitored for heart issues.

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

A 5-year-old girl has sparse, dry, and brittle hair but is otherwise healthy.

Researchers found a new mutation in the HR gene causing hair loss and skin bumps in a Pakistani family.

Glucocorticoids for progressive muscular dystrophy in children don't improve muscle strength or function but do increase certain side effects.

A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.

The fuzzy gene is crucial for controlling hair growth cycles.

ESR2 gene linked to female-pattern hair loss.

Hairless rats are good for testing anti-inflammatory drugs, similar to haired rats, without needing to remove fur.

PRP helps hair growth in common hair loss disorder.

Metreleptin treatment significantly improved metabolic health in a boy with congenital generalized lipodystrophy.

Proper antifungal treatment is crucial to avoid misdiagnosis and prevent scarring alopecia.

Cetaceans lost hair due to changes in the Hr and FGF5 genes.

A new MTX2 gene mutation caused a severe genetic disorder in a young Chinese girl.

Alopecia areata involves immune response and gene changes affecting hair loss.