congenital ichthyosis

congenital ichthyosis report :

Toxoplasmosis is a parasitic disease caused by the protozoan Toxoplasma gondii. Aphasia, is also known as aphemia, and is a loss of the ability to produce and Marfan syndrome is an autosomal dominant genetic disorder of the connective tissue characterized by disproportionately long limbs, long thin fingers, a typically tall stature, and a predisposition to cardiovascular abnormalities, specifically those affecting the heart valves and aorta. Schistosomiasis is a parasitic disease caused by several species of fluke of the genus Schistosoma. Weber syndrome, sometimes referred to as congenital ichthyosis encephalotrigeminal angiomatosis, is an extremely rare congenital neurological and skin disorder. or comprehend language, due to injury to brain areas specialized for these functions, Broca's area, which governs language production, or Wernicke's area, which governs the interpretation of language. . Classically, patients with LI are born as collodion babies encased in a plasticlike membrane that, within. Traditionally, ARCI patients are classified as having either lamellar congenital ichthyosiform erythroderma with fine whitish scaling on an erythrodermal background Rhinophyma is a descriptive term for a large, bulbous, ruddy appearance of the nose caused by granulomatous infiltration. Osteomyelitis is an infection of bone or bone marrow, usually caused by pyogenic bacteria or mycobacteria. Iritis is a form of anterior uveitis and refers to the inflammation of the iris of the eye. Cockayne syndrome is a rare, autosomal recessive disorder characterized by growth failure, impaired development of the nervous system, abnormal sensitivity to sunlight, and premature aging. Pityriasis rosea is a common, harmless human skin disease which presents as numerous patches of pink or red oval rash, mainly on the torso. Wilson's disease or hepatolenticular degeneration is an autosomal recessive genetic disorder in which copper accumulates in tissues