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A 23-year-old Syrian woman has two rare hair disorders, and avoiding hair treatments plus using vitamins and minoxidil may help.

All major hair defects involve cuticle abnormalities.

A 10-month-old boy with a rare combination of genetic conditions has severe immune deficiency and treatment challenges.

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

Hair dysplasias involve various hair disorders causing fragility, breakage, and poor hair adhesion.

Trichothiodystrophy causes unusual hair and developmental issues.

Dental erosion is common in adolescents and is linked to diet and higher socioeconomic status.

A new syndrome may link skin, growth, mental, and hair issues.

Recognizing bamboo hair helps diagnose Netherton’s syndrome.

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

Recognizing oral symptoms can help diagnose and treat blood and nutritional diseases early.

A rare case of trichothiodystrophy was found with autism, seizures, and mental retardation.

A child has a rare hair and skin disorder due to specific gene variants, suggesting broader genetic testing is needed.

Methionine intake changes tooth germ development in newborn rats.

Isolated patchy heterochromia with pili annulati can occur without other health issues.

Two siblings were the first reported cases of inheriting both eye coloboma and loose anagen syndrome together.

Sox21 is crucial for tooth development and enamel formation by preventing cells from changing into a different type.

The infant likely has Hay-Wells syndrome and needs genetic testing and heart screening.

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

About 38% of patients at a dermatology clinic had oral lesions, with coated tongue, fissured tongue, and Fordyce granules being most common.

Three siblings had both Vohwinkel's disease and congenital alopecia, with no effective treatment.

A young boy's uncombable hair is due to a rare genetic condition that usually improves over time.

The document explains how to identify different hair problems using a microscope.

Identical twins with a rare KRT 86 gene mutation both have the hair disorder monilethrix.

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

Edar and Eda proteins are crucial for proper tooth development.

A new genetic mutation was found causing hair and eye issues in a boy.

A family was found with both Trichorhinophalangeal syndrome and Loose Anagen Syndrome, suggesting a genetic connection.

Trichothiodystrophy can be linked to urologic issues and high calcium in urine.

A 4-year-old girl has a rare hair condition causing fragile, short hair.