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Human hair follicle organ culture is a useful model for hair research with potential for studying hair biology and testing treatments.

The document concludes that understanding hair structure is key to diagnosing hair abnormalities and recommends gentle hair care for management.

Hair, teeth, and mammary glands develop similarly at first but use different genes later.

Inherited ichthyoses cause widespread skin scaling and thickening due to gene mutations.

New LPA receptors (LPA4, LPA5, LPA6) have diverse roles in the body.

Trichoscopy is good for diagnosing and monitoring hair and scalp problems in children but needs more research for certain conditions.

Boys with less severe EDA mutations in XLHED have milder symptoms and better sweat and hair production.

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.

Black women's unique hair characteristics and styling practices can lead to specific scalp conditions, which require early diagnosis and appropriate treatment.

Trichoscopy can effectively tell apart tinea capitis and alopecia areata in children by looking for specific hair shapes.

Hairless protein is crucial for healthy skin and hair, and its malfunction can cause hair loss.

Gata6 is important for protecting hair growth cells from DNA damage and keeping normal hair growth.

The document concludes that veterinary dermatologists need more experience and a better approach to treating skin diseases in nonhuman primates.

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.

The review concludes that accurate diagnosis of different types of hair loss requires proper biopsy techniques and understanding the hair growth cycle and underlying causes.

A new PAX9 gene mutation causes missing teeth and hair problems, but not skin or nail 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.

The document concludes that oral finasteride and topical minoxidil are effective for genetic hair loss, while other treatments for different types of hair loss show promise but need more research.

Patients with chronic renal failure on hemodialysis often have skin problems like dry skin, itching, and nail changes.

The G60S Connexin43 mutation causes hair growth issues and poor hair quality in mice, similar to human ODDD patients.

New treatments and early diagnosis methods for permanent hair loss due to scar tissue are important for managing its psychological effects.

Vitamin D receptor helps control hair growth genes in skin cells.

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.

New hair loss treatments may include topical medications, injections, and improved transplant methods.

Taking Propecia might lead to the development of cataracts.

Scalp involvement in pemphigus means the disease is more severe and harder to treat.

Using methods like lasers and microneedling with drugs can improve hair regrowth for alopecia, but more research is needed on safety and best practices.

Latanoprost eye drops may cause skin depigmentation.

Boxer and Labrador dogs' hair growth is affected by the tropical climate, but Schnauzers' is not.

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.