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A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.

Not having enough or having too much of the protein Grainyhead-like 3 leads to various developmental problems.

Mice with the 'lanceolate hair' mutation have abnormal hair and skin similar to human Netherton's syndrome.

Newer low-dose oral contraceptives with less androgenic effects improve patient compliance.

A girl with a rare syndrome had successful hair loss treatment with no relapse after 4 years.

A child with skin and heart issues had rare genetic mutations affecting skin and heart cell cohesion.

A 12-year-old boy with twenty nail dystrophy, a condition affecting all nails, was treated conservatively due to its self-limiting nature and good prognosis.

Many women with seborrheic dermatitis also have acne and diabetes, and should be checked for these conditions to help improve their quality of life.

Infants with severe KID syndrome may be more prone to serious infections and need close monitoring.

Tight traditional hairstyles can cause hair loss.

A 9-year-old boy had a rare scalp condition usually seen in young men.

Treating gum disease and stress may help improve alopecia.

The document describes previously unreported unique skin changes in a rare genetic disorder called Hereditary mucoepithelial dysplasia.

Obesity leads to physical, metabolic, reproductive issues, higher healthcare costs, and mental health problems.

A 33-year-old woman with PCOS and metabolic syndrome was unusually diagnosed with a bone condition called DISH, suggesting a possible link between these conditions.

Vitamin D affects Msx1 protein expression and may influence mineralized tissue health.

Misdiagnosis of hair and scalp disorders is common in patients with skin of color, highlighting the need for better training and evaluation.

Higher BMI, IGF-1, and DHEAS levels are linked to advanced bone age in young Chinese girls with early breast development.

Noggin gene inactivation causes skeletal defects in mice, varying by genetic background.

A 3-year-old boy was diagnosed with a rare, non-scarring hair loss condition called temporal triangular alopecia.

The boy's symptoms suggest a possible new medical condition.

A woman with a rare form of multiple myeloma had a headache and a skull mass, which led to her diagnosis after tests and a biopsy.

Congenital atrichia with papular lesions causes permanent hair loss and skin bumps due to a gene mutation.

Skin problems in patients with polycystic ovarian disease are linked to body weight, blood sugar, and hormone levels.

Routine eye exams may be needed for alopecia areata patients due to common eye issues.

If a child is losing a lot of eyelashes and it keeps happening, doctors should look carefully at their health history because it might be a sign of a different health problem.

Composite flaps are better than muscle-only flaps for long-term skull coverage.

PCOS is common in women, often treated with lifestyle changes and oral contraceptives.