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Liver disease is linked to hair loss, especially in women and those with unhealthy lifestyles.

An elderly woman's upper lip lump, thought to be a mucocele, was actually a rare type of lymphoma usually found on legs, treated successfully with chemotherapy and radiation.

Patients with systemic lupus erythematosus and hair loss had non-scarring alopecia with fewer hair follicles, and direct immunofluorescence did not help identify lupus.

Systemic mastocytosis may cause a type of hair loss called cicatricial alopecia.

Two boys developed a viral skin infection during chemotherapy, which resolved with improved immune function.

A patient with a rare chromosome condition also had a rare type of hair loss.

Generalized trichoepitheliomas with hair loss may indicate myasthenia gravis.

Skin biopsy is crucial for diagnosing unknown baldness causes.

Early diagnosis and multidisciplinary care, including orthopedic surgery, can prevent long-term disability in IFAP syndrome.

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

A 21-month-old boy has a rare genetic disorder causing sparse hair due to an LSS gene mutation.

A Doberman Pinscher had a rare form of autoimmune disease causing hair loss and other severe symptoms.

Metastatic cervical cancer can cause rare, severe Cushing's syndrome with high risk of death.

Clouston Syndrome can be linked to rare sweat gland tumors.

These hair loss conditions might be part of a spectrum, not separate issues.

Björnstad syndrome can cause hair loss similar to androgenetic alopecia, and treatment with baricitinib and minoxidil may help.

NBCCS and BFHS might be the same syndrome, helping better identify and manage cases.

A new mutation in the XEDAR gene might cause a rare skin condition called hypohidrotic ectodermal dysplasia.

The lanceolate hair-J mutation in mice helps understand human hair disorders like Netherton's syndrome.

A Turkish family with sparse hair and eyebrow loss has a mutation in the U2HR gene linked to Marie Unna hereditary hypotrichosis.

Cri-du-chat syndrome can cause skin and oral lesions affecting nutrition and quality of life.

Accurate diagnosis is crucial for effective treatment of similar hair loss conditions.

Pimozide treatment resolved cysts and partially restored cheek fat in a man with Barraquer–Simons syndrome.

A 7-year-old girl was diagnosed with trichothiodystrophy due to low sulfur levels in her hair.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

A genetic mutation in the SGK3 gene causes hairlessness in Scottish Deerhounds and may relate to human hair loss.

Hair removal with intense pulsed light can cause rare skin lesions that are hard to fully treat.

A child with ectodermal dysplasia-syndactyly syndrome has a new mutation in the NECTIN4 gene.