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The patient with lupus and Degos' disease showed significant improvement with treatment.

Platelet-rich plasma (PRP) significantly improves long-lasting post-viral smell dysfunction.

Iron deficiency anemia can cause hair breakage.

Monkey lips have dense sensory nerves similar to those in other skin areas, explaining their sensitivity.

Early diagnosis and genetic evaluation of ADULT syndrome are crucial to reduce stress and medical costs.

A 19-month-old Saudi girl had a rare skin condition with no other defects, and her family was unaffected.

Early diagnosis and multidisciplinary care are crucial for improving the quality of life in patients with ectodermal dysplasia.

The hair defect is due to abnormal inner root sheath keratinization.

Neural cell nanovesicles help hair growth by activating key signals.

Selenium and iodine deficiencies cause delayed growth and abnormal neural behavior in rats.

An 18-year-old man was diagnosed with a rare genetic disorder causing hair loss, severe light sensitivity, and skin issues.

New mutations in the DSG4 gene cause a rare hair condition.

DPR can cause skin, hair, and nail issues, sometimes appearing later in life.

Restoring nerve-macrophage communication may help treat autoimmune diseases.

Light can activate hair growth through a pathway from the eyes to hair follicles.

Obstructive sleep apnea can be hereditary and linked to a genetic mutation in the COL1A2 gene.

Mutations in NIPAL4 cause skin issues by disrupting lipid layers, but some improvement is seen with topical treatment.

EPDS can cause recurring scalp sores and hair loss if not treated.

Epidermal nevi are skin cell clusters linked to various syndromes.

A 2-year-old girl with a rare vitamin D disorder had rickets and hair loss, but treatment was ineffective due to poor compliance.

Scientists created a cell model to study and find treatments for a skin disease called RDEB.

Increased scalp sweating in frontal fibrosing alopecia may be linked to local skin inflammation.

A direct brow lift can effectively fix nerve damage and improve appearance after surgery.

FOXN1 mutations can cause varying immune and physical issues, with severity influenced by gene activity and possibly other factors.

A new gene mutation causes a rare type of hair loss.

Certain genetic changes in the LSS gene cause a rare skin and hair condition.

A mutation in mice causes hair loss and skin issues due to a defect in a gene affecting cell adhesion.

Implanted dermal papillae can induce hair growth in rat ear wounds.

Rothmund-Thomson syndrome type 2 can cause chronic, poorly healing wounds.