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Becker's Nevus Syndrome is a rare condition with a skin patch and possible bone and muscle abnormalities, treated mainly for appearance.

Temporal triangular alopecia is a lifelong condition with hairless patches on the side of the head that may be present from birth.

Mutations in the androgen receptor gene cause Androgen Insensitivity Syndrome, affecting sexual development.

The report concludes that atypical Brauer nevus is more common in males, present at birth, and often misdiagnosed due to its unusual scalp locations.

Sebaceous glands are involved in various skin disorders, some treatable with medications like finasteride and minoxidil.

New markers and pathways have been found in skin tumors, helping better understand and diagnose them.

The document reports findings on genetic research, including ethical concerns about genome editing, improved diagnosis of mitochondrial mutations, solving inherited eye diseases, confirming gene roles in epilepsy, linking a gene to aneurysms, and identifying genes associated with age-related macular degeneration.

A 21-year-old male has a benign skin condition called Becker's nevus, which he chose not to treat.

Understanding normal hair growth and loss in children is key to diagnosing and treating hair disorders.

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

Both vitiligo and alopecia areata involve an immune response triggered by stress and specific genes, with treatments targeting this pathway showing potential.

The newborn with Klippel-Trénaunay syndrome was healthy but needed regular check-ups for possible complications.

Congenital triangular alopecia is a hair loss condition present from birth or early childhood with no effective treatment needed.

5% topical minoxidil effectively treated a boy's congenital triangular alopecia without side effects.

Congenital triangular alopecia is a harmless, non-spreading hair loss condition often seen in young children.

Hair problems can be caused by genetics or the environment, and treatment should focus on the cause and reducing hair damage.

The document concludes that doctors should recognize congenital triangular alopecia to avoid unnecessary treatments, as it does not respond to steroids like alopecia areata does.

Most cases of Temporal Triangular Alopecia are found in early childhood and may be related to genetic conditions.

The document concludes that early diagnosis and treatment are crucial for children with hair loss to prevent permanent damage, although not all conditions can be effectively treated.

CTA is often mistaken for AA but doesn't respond to steroids and may require hair transplantation.

A baby boy had two types of temporary hair loss at birth, which might be two forms of newborn hair loss combined.

Researchers found a genetic link for hereditary hair loss but need more analysis to identify the exact gene.

A 13-year-old boy had a rare, stable type of hair loss with little chance of regrowth, but treatment is available for looks.

Temporal triangular alopecia is a non-scarring hair loss in children, often linked to other health conditions.

Congenital triangular alopecia can occur outside the typical fronto-temporal region.

A 23-year-old man has a benign, non-progressive hair loss patch that doesn't respond to treatment but can be cosmetically treated.

A 5-year-old boy was diagnosed with congenital triangular alopecia, a type of hair loss without skin changes, usually starting between ages 2-5, with no specific treatment.

Epidermal nevi are skin cell clusters linked to various syndromes.

The chapter explains common scalp conditions, including infections, infestations, and tumors.

Congenital triangular alopecia and vitiligo can occur together, but treatment for one may not affect the other.