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Recognizing minor skin lesions can help identify serious cancer syndromes.

PC-associated alopecia has unique microscopic features.

A 12-year-old boy in rural south India had a rare skin condition causing hair loss and inability to sweat.

Somatic BHD mutations are rare in Japanese renal tumors.

Alopecia triangular temporal is a rare condition with unclear causes and treatment, but trichoscopy helps in diagnosis.

Mutations in the TSPEAR gene cause a new form of ectodermal dysplasia affecting hair and tooth development.

Trichostasis spinulosa is a common but often unnoticed skin condition involving bundled vellus hairs, especially in people with darker skin or UV exposure.

People with myotonic dystrophy type 1 tend to develop basal cell carcinoma at a younger age but not more frequently than others.

A severe form of Netherton syndrome caused by a specific gene mutation led to neonatal deaths in a family.

Common variants in the Trichohyalin gene are linked to straight hair in Europeans.

A man with both Klinefelter syndrome and primary hyperparathyroidism showed a rare combination of symptoms and genetic patterns.

Consider rare forms of CAH for accurate diagnosis and treatment.

A child with trichothiodystrophy also had autoimmune thyroiditis and anemia, which is a new finding.

The conclusion is that the variation in hair thinness in patients is mostly due to the amount of underdeveloped hairs, and treatments that thicken fine hairs might work for those with mild to severe conditions.

Norfolk Terriers have a genetic skin defect causing scaling and blisters due to a keratin issue.

Corticosteroids improved symptoms in a man with Cronkhite-Canada Syndrome.

DSDs are birth conditions causing unusual sex development, managed with personalized care and sometimes surgery, but still lack a standard treatment approach.

Children with Turner Syndrome often have skin, hair, and nail issues linked to hormonal problems, so regular skin checks are recommended.

Comprehensive genetic testing and international collaboration are crucial for better understanding and managing Ehlers-Danlos syndromes.

A genetic variant in the GJB6 gene likely caused the Labrador's paw pad condition.

Older men's scalp damage increases with age and sun exposure, a baby girl in the Philippines has Schimmelpenning syndrome, and thyroid screening is advised for children with hair loss and certain risk factors.

Rabbits lacking the Hoxc13 gene show similar hair and skin issues to humans with ECTD-9, making them good for research on this condition.

Early diagnosis, genetic testing, and personalized care are essential for managing tuberous sclerosis.

Researchers found a new genetic mutation linked to a hair condition in a Japanese boy.

Mutations in the vitamin D receptor cause hereditary vitamin D-resistant rickets, leading to poor bone health and requiring high calcium doses for treatment.

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

People with Birt-Hogg-Dubé syndrome often have lung problems and delayed diagnosis, and better recognition of CT scan signs could improve diagnosis and management.

A man with four autoimmune diseases suggests a new category for multiple autoimmune syndrome.