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A man with a rare skin condition and a new gene mutation developed high calcium levels due to his treatment.

Trichoscopy helps diagnose and assess the severity of Frontal Fibrosing Alopecia.

Two siblings were diagnosed with Trichothiodystrophy, identified by brittle hair and low sulfur content.

Thermal imaging is a useful non-invasive method to diagnose active inflammation in frontal fibrosing alopecia.

Vitamin B12 deficiency can cause darkening of all nails.

A patient with Rothmund-Thomson syndrome showed skin changes, hair loss, and dental defects but no cataracts or skeletal issues.

The fractional ultrapulse CO2 laser is a safe and effective non-surgical treatment for upper eyelid issues and brow lifting.

People with Epidermolysis bullosa have many health problems including poor oral health, which is often neglected due to other medical issues.

Loss of Ten1 in mice causes telomere shortening and symptoms similar to human dyskeratosis congenita.

Vitamin-D and calcium effectively treat hair loss in children.

Bimatoprost can cause longer, thicker, darker eyelashes and eyebrows.

A rare autoimmune disease caused the woman's scalp blisters and hair loss, successfully treated with medication.

A Japanese patient with IFAP syndrome had a severe MBTPS2 gene mutation but showed milder symptoms than previously observed cases.

The system helps identify vitamin deficiencies early by analyzing symptoms.

People with Alopecia Areata have lower vitamin D levels.

An infant with a zinc deficiency skin disorder improved with zinc treatment.

The cornified envelope is crucial for skin's barrier function and involves key proteins and genetic factors.

Perifollicular erythema can indicate active frontal fibrosing alopecia.

Minoxidil may cause vision problems.

Women with menstrual dysfunction often have deficiencies in magnesium, iron, and vitamin D.

Low vitamin D levels, not ferritin levels, were found in patients with hair loss condition telogen effluvium.

Telogen effluvium is a common, temporary hair loss condition often affecting young women.

Discoid Lupus Erythematosus often causes scarring hair loss, is influenced by genetics and environment, and requires early treatment to prevent worsening.

Fluorescence can effectively measure acne treatment progress.

The boy's severe skin disorder is caused by two new mutations in his TGM1 gene.

An artificial lipid barrier can restore hair growth in cases of SCD1 deficiency.

The combination therapy significantly improved Riehl’s melanosis in patients without serious side effects.

Targeted siRNA therapy may be a promising treatment for KID syndrome by reducing mutant gene expression and improving cell communication.

Finasteride may cause cataracts and floppy-iris syndrome.

The man has a genetic skin condition called pachyonychia congenita.