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Porphyria cutanea tarda causes skin issues due to an enzyme deficiency.

A man with total hair loss developed blackhead-like spots on his scalp, possibly because no hair was present to help drain oils.

The document concludes that detailed clinical descriptions of seven family cases help understand dominant dystrophic epidermolysis bullosa's symptoms and inheritance.

Genetic testing confirmed a young girl has Atrichia with Papular Lesions due to mutations in the hairless gene.

The article helps identify common, non-harmful skin conditions in newborns to avoid undue concern and treatment.

Most skin conditions in Down syndrome are benign and involve dry or thickened skin.

Acne can appear or persist in adulthood due to hormonal changes, external factors, or substance use, and requires appropriate treatment.

Dermoscopy helped correctly diagnose a skin condition that was previously misidentified as a different hair loss disease.

Dermoscopy has improved skin cancer diagnosis and has expanding applications in dermatology, but requires staying updated with new research and techniques.

A patient with Sézary syndrome showed improvement after treatment and the study suggested follicular mucinosis might indicate future lymphoma risk.

A new classification system for skin cysts was proposed to improve diagnosis.

Trichoepitheliomas can be hard to distinguish from other skin conditions and often start in teenage years.

The research linked PLCD1 gene variants to the development of trichilemmal cysts.

A new gene mutation caused a man's rare skin condition, Schöpf-Schulz-Passarge syndrome.

The document explains the genetic causes and characteristics of inherited hair disorders.

The baby’s hair loss was due to a rare genetic condition, not treatable by usual methods.

Early diagnosis and treatment of hereditary vitamin D-resistant rickets (HVDRR) are crucial to prevent growth issues and other health problems.

Folliculotropic mycosis fungoides has a worse prognosis than other types, with survival rates varying significantly based on subtype and organ involvement.

An 8-year-old girl has a rare, irreversible hair loss condition caused by a genetic mutation.

Melanocyte transplantation can safely restore skin color, especially in stable vitiligo, but must be chosen carefully based on the disease phase.

Benign skin tumors need accurate diagnosis to ensure proper treatment.

Different types of hair loss in dogs and cats have various causes and treatments, with outcomes ranging from good to uncertain.

Spironolactone use is not linked to an increased risk of breast cancer, but caution is advised for high-risk patients.

A woman's skin symptoms led to a diagnosis of systemic AL amyloidosis, but she died from sepsis shortly after.

Certain skin diseases are linked to Agent Orange and similar chemicals; veterans should be screened and informed about uncertain risks, and current data doesn't link spironolactone with breast cancer.

Skin changes throughout life, from development before birth to aging effects like wrinkles, influenced by both genetics and environment.

Alopecia in animals can be hereditary, congenital, or acquired, with treatments and outcomes varying widely.

Most patients with Tuberous sclerosis had neurological or skin issues, and over half had psychiatric problems.

Yellow dots look different in various hair loss conditions and can help diagnose them.

A man with Klinefelter syndrome had a leg ulcer that didn't heal well, even with treatment.