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Older patients with new retinal lesions may have cancer, and local radiation might not stop it from spreading.

CARASIL, a rare genetic disorder, was confirmed in an Arabic woman, highlighting its rarity and need for stroke prevention.

Most treatments for lichen planopilaris were found to be generally unsatisfactory.

Premature graying of hair is common and stressful, but not well understood or treated.

Tight hairstyles can cause a rare scalp condition with thick skin folds.

A unique type of lupus panniculitis causes reversible hair loss on the scalp in East Asians.

Mutations in the LSS gene cause a rare type of hereditary hair loss.

A child with a rare scalp condition regrew hair after treatment.

Two children with lysinuric protein intolerance showed symptoms similar to lupus.

NKG2D gene polymorphism doesn't affect SLE risk but may influence symptoms like rash and hair loss.

PC-associated alopecia has unique microscopic features.

A new TP63 mutation was found in a baby with EEC syndrome, showing the need for TREC testing to check for immune issues.

People with Lichen planopilaris are more likely to have certain autoimmune and endocrine disorders but less likely to have conditions like allergies and diabetes.

A new mutation in the human glucocorticoid receptor reduces its function and causes resistance to glucocorticoids.

Pseudopelade of Brocq is hard to diagnose and treat, with limited effective options.

The patient has Chronic Cutaneous Lupus, a skin condition causing plaques and hair loss.

Lichen planopilaris (LPP) is linked to androgen excess, while frontal fibrosing alopecia (FFA) is linked to androgen deficiency.

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.

LIPH mutations in Japan cause varying degrees of hair loss and woolly hair.

Skin lesions in Carney Complex are caused by a gene change in some skin cells that leads to increased pigmentation and may lead to tumors.

A woman with lupus and severe nerve damage improved with specific treatments.

Primary idiopathic pseudopelade of Brocq causes gradual, scarring hair loss with no effective treatment.

The Swedish neonatal screening program effectively detects PKU, galactosaemia, and biotinidase deficiency with low false positives.

Hyperaesthetic leucotrichia in horses causes painful, recurring skin lesions and hair color changes, especially in Arabian and American paint horses.

The HSD3B1 variant increases hair loss risk in overweight women with PCOS.

Higher ꝩ-GCS enzyme levels in PCOS patients may play a role in the disease.

The document concludes that Loose Anagen Hair Syndrome is a benign condition where hair is thin and easily pulled out, often improving with age.

Restoring phenylalanine levels improved skin and hair symptoms in a PKU infant.

The skin condition Ulerythema ophryogenes did not improve with treatment in a patient with other birth defects.

A gene mutation causes woolly hair in a Syrian patient.