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The Hairless gene is crucial for hair cell development, affecting whether skin cells become hair or skin and oil gland cells.

Mutations in the PTPRQ gene cause significant balance issues in mice due to hair bundle defects in the inner ear.

Children's hair loss can be caused by many factors, including autoimmune diseases, emotional stress, genetics, and infections, with treatment and prognosis varying.

Researchers made a mouse model with curly hair and hair loss by editing a gene.

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

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

The review shows that skin symptoms like chronic fungal infections, hair loss, and skin depigmentation are key for early detection and management of APECED.

Patients with the same genetic mutation for vitamin D-resistant rickets showed different symptoms but all improved with treatment except for hair loss.

A 5-year-old girl has sparse, dry, and brittle hair but is otherwise healthy.

Early diagnosis and tailored treatments are crucial for managing ichthyosis syndromes with hair abnormalities.

Non-ablative and ablative fractional lasers helped hair growth in some cases without major side effects, but didn't work for all hair disorders.

The update highlights that non-classic congenital adrenal hyperplasia is common in women with excess male hormones, requires specific hormone tests for diagnosis, and has various treatment options depending on age and symptoms.

A cross-bred lamb with severe skin and movement issues had ichthyosis fetalis but normal vitamin A levels.

Leptin-deficient mice, used as a model for Type 2 Diabetes, have delayed wound healing due to impaired contraction and other dysfunctional cellular responses.

An infant with a zinc deficiency skin disorder improved with zinc treatment.

RANK is a key target in breast cancer treatment due to its role in tumor growth and bone metastasis.

The boy's severe skin disorder is caused by two new mutations in his TGM1 gene.

Vitamin D3 and its receptor are important for hair growth, and understanding receptors could help treat hair graying and skin cancer.

Early diagnosis and treatment of NCCAH can improve symptoms and fertility.

A 4-year-old boy with a rare type of rickets and hair loss improved in bone health but not hair growth after vitamin D and calcium treatment.

Experts discussed treatments for skin conditions in children, emphasizing hydration, cautious medication use, and early intervention for infections.

sPLA2-X is crucial for normal hair growth and follicle health.

CaBP1 and CaBP2 are necessary for proper hearing and neurotransmission in the ear's inner hair cells.

The fuzzy gene is crucial for controlling hair growth cycles.

ESR2 gene linked to female-pattern hair loss.

Hairless rats are good for testing anti-inflammatory drugs, similar to haired rats, without needing to remove fur.

The same genetic mutation in Sjögren-Larsson syndrome can lead to different levels of severity, suggesting other factors influence the symptoms.

A patient with sickle cell trait and low vitamin D might have lupus, a rare combination that needs more attention.

A baby with a rare metabolic disorder developed a rash not cured by zinc alone, likely due to both zinc and amino acid deficiencies.

Metreleptin treatment significantly improved metabolic health in a boy with congenital generalized lipodystrophy.