Search

everythinglearnresearchcommunity

for

Search:↓

Certain genetic changes in the LSS gene cause a rare skin and hair condition.

Mice with LSS deficiency showed hair loss and cataracts, similar to humans, and can help in understanding and treating this condition.

The document emphasizes the importance of correctly identifying and classifying genetic hair disorders to help diagnose related health conditions.

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

Most hair loss in children is caused by a few common conditions, and it's important to diagnose these properly and support the child's mental health.

Injecting triamcinolone into the eyebrow area may help eyelash regrowth in alopecia areata patients.

Transverse sections are better for non-scarring hair loss, vertical sections are better for lichen planopilaris, and either method works for other scarring hair loss types.

Mutations in the LSS gene cause a rare type of hereditary hair loss.

The study found no common cause for a girl's crystalline cataract and uncombable hair, suggesting their co-occurrence might be coincidental.

Aquaporins could be new drug targets for treating polycystic ovary syndrome.

Stress, nutritional issues, and chronic diseases can cause hair loss, and nail changes may signal internal diseases; treatment focuses on the underlying cause.

The document explains the genetic causes and characteristics of inherited hair disorders.

Changes in the SREBF1 gene cause a rare genetic skin and hair disorder.

Mutations in mitochondrial DNA might significantly contribute to the development of Polycystic Ovarian Syndrome.

People with Down syndrome have higher rates of certain immune-related conditions and need special medical attention.

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

Diabetes can lead to blindness and skin problems, and managing blood sugar and blood pressure is crucial to prevent these complications.

The document concludes that eyelash trichomegaly, which is the abnormal growth of eyelashes, can be present from birth, caused by diseases, or result from certain medications.

Acitretin helped improve hand mobility and skin condition in a patient.

Bovines can have rare inherited skin diseases with specific symptoms like hair loss, fragile skin, and abnormal porphyrin buildup.

Some congenital hair disorders improve in childhood or with treatments like minoxidil and retinoids, while others like Netherton syndrome and trichothiodystrophy have a poor prognosis.

Some congenital hair disorders improve with age and can be managed with treatments like minoxidil, retinoids, supplements, and gentle hair care, but there's no cure.

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

Tiger cubs fed artificial milk lacking certain amino acids developed eye problems and hair loss.

Taking Propecia might lead to the development of cataracts.

Pili torti is a rare condition where hair is twisted and breaks easily, often linked to genetic disorders or other health issues.

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.

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.

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.

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.