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Babies born after 38 weeks to mothers under 36 years old and not delivered by C-section have a higher risk of neonatal occipital alopecia.

The document says that there are treatments for hair and nail diseases.

Dermoscopy is useful for identifying and tracking different types of hair loss without scarring.

The document reviews various hair and nail disorders, their causes, and treatments, emphasizing the need for proper diagnosis and the link between nail changes and systemic diseases.

Wnt1a helps keep cells that can grow hair effective for potential hair loss treatments.

New genetic mutations linked to rare skin disorders were found in three newborns.

Isotretinoin effectively treated a rare scalp condition, but careful drug monitoring and a dairy-free diet were important.

A woman's hair loss and other symptoms were due to a rare hormone deficiency treatable with steroids.

A rare skin condition with dark, thick, warty patches and some hair loss was found in a newborn boy.

A 21-day-old baby had a skin rash that didn't improve with cream and wasn't caused by a fungus.

Automated image analysis helps diagnose and monitor alopecia areata by efficiently measuring hair follicles.

Dietary lipids affect inflammation and are crucial for normal cell function and immune health.

UVB is good for a skin condition in Asian kids, a lotion works for head lice, a drug helps with a skin blistering disorder, a foam reduces itchiness in skin inflammation, birthmarks can be more widespread, and criteria for a neurocutaneous disorder were agreed upon.

UVA1-light therapy successfully treated a child's skin condition, mycosis fungoides.

Dermoscopy is becoming essential for diagnosing skin conditions and is expected to be a standard tool for dermatologists.

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.

A rare EGFR mutation in newborns leads to severe health issues and early death.

Genetic hair shaft abnormalities can be seen with microscopes and often affect scalp hair.

Thyroid hormones are important for skin health and changes in them can affect conditions like hair loss and eczema.

A baby from an Indian family had a rare genetic disorder causing no scalp or body hair due to a specific gene deletion.

Acne in children varies by age and severity, requires a pediatric treatment approach, and may need diagnostic evaluation for underlying conditions.

Doctors need more training in skin cancer screening, a new treatment is effective for a skin condition, better diagnosis methods for skin cancer are available, hair loss in women may be linked to hormones and cholesterol, certain skin care products might cause hair loss, babies' skin gets weaker after birth, and a gene mutation might be linked to eczema.

A woman had both Graham Little-Piccardi-Lassueur syndrome, causing hair loss, and complete androgen insensitivity syndrome, making her genetically male but physically female. This suggests androgens don't affect the hair loss condition.

Half-siblings with a rare skin condition improved with treatment for a fungal infection, but hair loss remained.

Probiotics may help treat skin conditions like acne and eczema safely.

Monilethrix is a rare, inherited condition causing fragile hair and hair loss, with no cure but some treatments may help.

A person was born with both a rare hairless condition and a type of birthmark, which is an uncommon combination.

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

Hutchinson-Gilford Progeria Syndrome is a rare genetic disorder caused by a specific gene mutation, characterized by aging symptoms and managed by monitoring heart health and using low-dose aspirin.

Trichohyalin is found in non-hair tissues and works with filaggrin in certain skin areas and conditions.