Articles, tagged with "juliet cohen", page 3

Harlequin Ichthyosis

Harlequin ichthyosis also known as Harlequin Type Ichthyosis. Harlequin ichthyosis is characterized by a thickening of the keratin layer in fetal human skin. Infants with this condition are born with very hard, thick skin covering most of their bodies. Th... Read >
Author: Juliet Cohen

Hantaviruses

Hantaviruses are a group of viruses found in wild rodents. Hantaviruses are a family of viruses that can lead to bleeding in the lungs and kidney damage. Prior to the outbreak in the southwestern United States, they were best known to cause disease from W... Read >
Author: Juliet Cohen

Halo naevi

Halo naevi, also known as leukoderma acquisitum centrifugum. Halo nevi are common benign skin lesions that represent melanocytic nevi in which an inflammatory infiltrate develops, resulting in a zone of depigmentation surrounding the nevus. They appear as... Read >
Author: Juliet Cohen

Hairy tongue

Hairy tongue, also known as black tongue, is a gentle condition of elongation and staining of the fingerlike projections (papillae) on the tongue surface. This condition may be caused by overgrowth of a bacteria or yeast that produces a colored substance.... Read >
Author: Juliet Cohen

Hailey-Hailey disease

Hailey-Hailey disease is also known as familial benign chronic pemphigus. Hailey-Hailey disease is a rare disease of the skin. It can begin at any age, but it is most common in the late teenage years, twenties and thirties. Typically it appears as thin wa... Read >
Author: Juliet Cohen

Gigantomastia Detailed Information

Gigantomastia (also known as macromastia) is a condition in which a woman's breasts cultivate to too much size, usually as a consequence of pregnancy. The condition is caused by over-sensitivity to the woman hormones estrogen and progesterone, and/or an u... Read >
Author: Juliet Cohen

Giant axonal neuropathy (GAN) Detailed Information

Giant axonal neuropathy (GAN) is a degenerative disorder of the peripheral nerves that is inherited as an autosomal recessive attribute, presenting in early childhood and progressing to death, usually by late adolescence. Giant axonal neuropathy is caused... Read >
Author: Juliet Cohen

Gianotti-Crosti syndrome Detailed Information

Gianotti-Crosti syndrome (GCS) is a different contagious exanthem with related lymphadenopathy and acute anicteric hepatitis. Gianotti-Crosti Syndrome is a rare skin disease affecting children between the ages of nine months and nine years. More than 90% ... Read >
Author: Juliet Cohen

Galactokinase deficiency Detailed Information

Galactokinase deficiency, also known as Galactosemia type 2 or GALK deficiency. Galactokinase deficiency (GKD) is an inherited disorder of galactose metabolism. It is characterized by galactosuria and galactosemia that is caused by a deficiency of the gal... Read >
Author: Juliet Cohen

Fucosidosis Types 1 Detailed Information

Fucosidosis is inherited as an autosomal recessive genetic trait. Fucosidosis is a really uncommon hereditary lysosomal storage disease characterized by a deficiency of the enzyme alpha-L-fucosidase. This disorder belongs to a group of diseases known as l... Read >
Author: Juliet Cohen

Fox-Fordyce disease Detailed Information

Fox-Fordyce disease is an rarely happing chronic pruritic papular eruption that place to areas where apocrine glands are create. This condition is also referred to as ‘apocrine duct occlusion' and ‘sweat retention disease'. Fox-Fordyce disease is most... Read >
Author: Juliet Cohen

Fissured tongue Detailed Information

Fissured tongue, also called scrotal tongue. Fissured tongue is a benign condition characterized by deep grooves (fissures) in the dorsum of the tongue. The surface furrows may differ in size and depth, radiate outward, and cause the tongue to have a wrin... Read >
Author: Juliet Cohen

Complete Information on Ablepharon macrostomia syndrome with Treatment and Prevention

Ablepharon macrostomia syndrome is an exceedingly uncommon inherited hereditary disorder. The precise reason of Ablepharon macrostomia syndrome is not amply understood, some cases indicate that the disorder may be inherited as an autosomal recessive hered... Read >
Author: Juliet Cohen

Complete Information on Cretinism

Cretinism is a circumstance of seriously stunted physiological and psychological increase payable to raw inborn inadequacy of thyroid hormones. Cretins have dwarfed bodies, with curvature of the backbone and pendulous stomach. Their limbs are distorted, t... Read >
Author: Juliet Cohen

Complete Information on Cutis laxa

Cutis laxa too called elastolysis. It is a group of uncommon connective tissue disorders in which the rind becomes inelastic and hangs broadly in folds. Cutis laxa can be balmy, affecting simply an individual's show, or serious, affecting the domestic org... Read >
Author: Juliet Cohen

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