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A new severe form of monilethrix syndrome includes hair loss, scalp itching, cataracts, and distinct facial features.

The case suggests a possible link between severe acne and certain bone deformities.

Several genes, including Hox-7A, Stra6, and Lim-1, are involved in normal palate formation.

A child with Olmsted syndrome showed mild improvement in hair and skin issues with treatment.

Hand-foot-mouth disease may cause nail loss in children.

A mutation in the HOXC13 gene causes hair and nail problems in a Syrian family.

Mitochondrial problems in tooth cells lead to bad enamel and dentin development in mice.

Netherton's disease causes multiple hair defects.

A five-year-old girl has a harmless, unchanging bald patch on her scalp.

A rare benign cheek tumor was successfully removed from a 15-year-old girl without complications or recurrence.

The boy's symptoms suggest a possible new medical condition.

Genetic hair shaft abnormalities can be seen with microscopes and often affect scalp hair.

A genetic mutation in the CDH3 gene causes hair loss and vision problems in a young Saudi girl.

Congenital atrichia with papular lesions causes permanent hair loss in children.

The document concludes that AFA should be considered in patients with acromegaly-like features but normal hormone levels, and more cases need to be identified to understand the condition fully.

Using calvarial bone for maxilla augmentation is less painful and allows for single-procedure dental implants.

A 16-year-old girl with gum overgrowth and excessive hair growth had successful gum surgery and healed well.

Accurate diagnosis of APL is crucial to avoid unnecessary treatments.

HLD10 can include increased body hair and Mongolian spots.

Mutations in the DSG4 gene can cause a rare hair disorder similar to monilethrix.

The boy likely has a fungal infection causing hair loss.

An 11-year-old girl with hair thinning was diagnosed with monilethrix and early androgenetic alopecia.

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

Different harmful mutations in the CDH3 gene cause HJMD, but symptoms vary among individuals.

A 4-year-old girl has a rare condition causing hairlessness and skin bumps, but normal teeth and sweating.

Pili torti hair is fragile due to loose keratin filaments and weak disulfide bonds.

Airway issues can occur in Conradi–Hünermann–Happle syndrome and can be managed with minimally invasive procedures.

Monilethrix causes short, fragile hair with no specific treatment available.

The infant's hair loss resolved naturally by 20 months without treatment.

Anorexia nervosa may cause a hair defect called pili torti due to malnutrition and high vitamin A levels.