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Erosive palmoplantar lichen planus in North-East India mainly affects the feet and often involves nails, with unique inflammatory skin changes.

Overexpressing the glucocorticoid receptor in mice leads to abnormal skin development and reduced inflammation.

Lichen planopilaris can be accurately diagnosed and effectively treated.

Mutations in the glucocorticoid receptor gene cause reduced sensitivity to glucocorticoids and may lead to poor response to treatment.

Lichen planus pigmentosus may indicate undetected hepatitis C infection.

Hair dysplasias involve various hair disorders causing fragility, breakage, and poor hair adhesion.

A child with Olmsted syndrome showed mild improvement in hair and skin issues with treatment.

Repeated biopsies are crucial for managing lupus panniculitis when initial treatments fail.

Hormonal imbalances in Polycystic Ovarian Syndrome (PCOS) might trigger a rare skin disorder called Confluent and Reticulated Papillomatosis (CRP), so dermatologists should consider checking for PCOS in CRP patients.

Ixekizumab may be an effective first treatment for a rare skin condition causing hair loss.

The infant was diagnosed with Rothmund-Thomson syndrome, a rare genetic disorder causing various physical and developmental issues.

A patient with both bullous lichen planus and systemic lupus erythematosus showed improvement with treatment.

Higher PHGDH levels cause unusual melanin buildup in hair follicles.

PPARgamma is crucial for healthy hair follicles, and its loss causes scarring alopecia.

Skin lesions in Carney complex are likely caused by a specific group of skin cells that promote pigment production due to a genetic mutation.

Glypican-4 may help indicate insulin sensitivity and lipid issues in women with PCOS.

A 4-year-old girl had a rare hair disorder affecting only part of her scalp.

Fibrosing alopecia in a pattern distribution is a hair loss condition often confused with other types, requiring early treatment but usually not resulting in significant hair regrowth.

A person with Werner syndrome was initially thought to just have female pattern hair loss.

A person got uncombable hair syndrome from two copies of chromosome 1 from their mother.

The woman was diagnosed with lichen planopilaris and can be treated with corticosteroids.

Folliculin deficiency causes problems with cell division and positioning due to disrupted RhoA signaling and interaction with p0071.

Grasp protein helps maintain skin health after UVB exposure.

RSPO1 mutations in certain patients lead to skin cells that don't develop properly and are more likely to become invasive, increasing the risk of skin cancer.

Premature graying in young children can affect self-esteem, and addressing underlying health issues may reverse it.

The document reports a rare case of ECCL with a new association with optic disc colobomas.

Face transplant for a severe autoimmune disease patient was successful, improving appearance and function without disease relapse after three years.

People with cutaneous Lichen Planus are more likely to have Metabolic Syndrome and related conditions like high cholesterol, diabetes, and high blood pressure.

Treatment with moisturizers improved the skin condition of a girl with a rare genetic skin disorder.

A girl inherited excessive body hair from her mother and grandmother.