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The baby’s hair loss was due to a rare genetic condition, not treatable by usual methods.

Genetic testing is crucial for diagnosing congenital atrichia, a rare condition causing irreversible hair loss.

Hair transplantation is a surgical procedure to move hair to bald areas, requires good donor hair, and results show in about a year.

Alopecia areata incognita causes widespread hair loss without patches and needs a scalp biopsy for diagnosis.

A different gene near the hairless gene on chromosome 8p21 causes a rare hair loss condition in a German family.

FOXN1 gene mutations cause a rare, severe immune disease treatable with cell or tissue transplants.

Behavior therapy and medications, especially clomipramine, can help reduce hair pulling in people with trichotillomania.

Eyebrow transplantation can be successful for Asians with the right technique and care, but regular maintenance is necessary.

A boy with chromosome 13q deletion syndrome developed eye cancer, a woman with breast cancer lost vision due to a rare side-effect of her treatment, a man's vision worsened after using a hair loss drug, and two rare disorders were discussed. Optical Coherence Tomography is useful for diagnosing and monitoring these conditions.

Eye exams are crucial for kids with 13q deletion syndrome, tamoxifen can cause vision loss, Propecia may lead to cataracts, Lipoid Proteinosis causes skin bumps, and OCT is useful for diagnosing macular diseases.

Some patients with a type of skin lymphoma can experience a rare, non-scarring hair loss that looks like another hair loss condition but has distinct features.

A baby boy with 13q deletion syndrome had eye cancer, a woman's vision improved after stopping a breast cancer drug, a man developed cataracts from using Propecia, and a rare skin disorder called Lipoid Proteinosis was discussed. Also, a tool called OCT is useful for diagnosing macular diseases.

Taking Propecia might lead to the development of cataracts.

Successful eyebrow restoration can be done using careful hair transplant techniques and choosing the right patients.

The document discusses various eye conditions and their treatments, including a rare eye cancer in a baby, vision loss from a cancer drug, cataracts from a baldness treatment, a rare skin disorder, and a specific type of eye disease diagnosed with a special imaging technique.

Finasteride, often used for hair loss, can potentially cause cataracts.

The document concludes that careful diagnosis is crucial for chromosome 13q deletion syndrome, tamoxifen can cause reversible eye damage, finasteride may be linked to cataracts, and OCT is useful for diagnosing macular diseases.

Chemotherapy caused a woman's permanent hair loss and early menopause.

Multiple eye conditions were studied, highlighting the importance of various imaging methods for diagnosis, the vision side effects of drugs tamoxifen and Propecia, and the usefulness of optical coherence tomography for diagnosing and monitoring macular and retinal diseases.

Trichoscopy is essential for diagnosing and managing alopecia areata in children.

The document describes a rare case of IFAP syndrome, a genetic condition with symptoms of hair loss, light sensitivity, and scaly skin.

Adjusting the medication tacrolimus resolved a boy's red nail beds after a stem cell transplant.

Mother and son diagnosed with a rare genetic hair loss condition with no effective treatment.

The conclusion is that certain cell interactions and signals are crucial for hair growth and regeneration.

Alopecia areata causes hair loss, has no cure, and various treatments exist.

The document concludes that hair is complex, with a detailed growth cycle, structure, and clinical importance, affecting various scientific and medical fields.

Trichoscopy is a useful non-invasive method for diagnosing different hair loss conditions.

The FOXN1 gene is crucial for developing immune cells and preventing immune disorders.

Some breast cancer chemotherapy can cause permanent hair loss.

Some chemotherapy can cause permanent hair loss.