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Somatic BHD mutations are rare in Japanese renal tumors.

Steatocystoma multiplex is a skin condition starting around age 26, linked to hair follicles, and related to eruptive vellus hair cysts.

Generalized vitiligo in Chinese patients is linked to other autoimmune diseases, especially in familial cases.

Monilethrix severity varies and may be influenced by other genetic or environmental factors.

Hairy elbows may be linked to short stature, but the exact cause is unclear.

ERK activation spreads between cells, influencing cell division and wound healing.

A 2-year-old girl had a hair disorder not shared by her identical twin.

ERK activation spreads between cells in mouse skin, linked to cell division and influenced by TPA and EGF receptors.

Animal models help study psoriasis but have limitations and don't fully mimic the human disease.

Uncombable hair is inherited dominantly with complete penetrance.

The 736T>A mutation in the LIPH gene is common in Japanese people with autosomal recessive woolly hair.

A 6-year-old girl's inability to grow her hair long was due to Loose Anagen Hair Syndrome, which causes hair to shed easily and may improve with age.

Scientists found a new protein, AMY117, common in Alzheimer's patients, which could be important for treatment and diagnosis.

VHL disease can cause early paragangliomas, needing lifelong monitoring.

The dog had sebaceous adenitis, treated with ciclosporin, leading to some hair regrowth.

Finasteride effectively reduced priapism episodes in children with sickle cell disease without side effects.

Short Anagen Syndrome causes persistently short hair and increased shedding, usually improving after puberty.

A rare scalp infection in a child developed into a kerion with additional skin symptoms.

Trichodysplasia spinulosa is a rare skin condition caused by a virus, treatable with antiviral medication.

The condition is likely inherited in an autosomal-dominant pattern.

A rare form of alopecia causes hair thinning without bald spots and may be more common than thought, responding well to steroid treatment.

A man with a weakened immune system was diagnosed with a rare skin condition called trichodysplasia spinulosa using skin examination techniques.

Lichen spinulosus, usually seen in young people, can rarely occur in adults, as shown by a 52-year-old woman with a rough, bumpy rash.

Trichodysplasia spinulosa is a rare skin disease in immunocompromised patients caused by a specific virus targeting hair follicle cells.

Trichodysplasia spinulosa is a rare skin condition linked to weakened immune systems, mostly in organ transplant patients.

Less than a quarter of alopecia areata cases were unusual forms or had paradoxical regrowth.

The early genes of a specific virus can cause abnormal skin cell growth and hair follicle changes.

Minoxidil treatment can reduce hair shedding, increase hair volume, and even change hair color in patients with loose anagen hair syndrome.

Some cases of folliculotropic mycosis fungoides may progress slowly and not need aggressive treatment.

A rare skin condition was confirmed to be associated with a specific virus in a young girl.