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The congenital mirror movements begin in infancy and persist throughout the patient's life, often with very little improvement, or deterioration. [3] Consequently, patients with this movement disorder have serious difficulty carrying out tasks that require manual dexterity or precision, such as playing a two handed musical instrument or typing ...
Ulnar dimelia, also referred to simply as mirror hand, is a very rare congenital disorder characterized by the absence of the radial ray, duplication of the ulna, duplication of the carpal, metacarpal, and phalanx bones, and symmetric polydactyly.
Congenital adrenal hyperplasia (CAH) Congenital central hypoventilation syndrome; Congenital diaphragmatic hernia (CDH) Congenital Disorder of Glycosylation (CDG) Congenital hyperinsulinism; Congenital insensitivity to pain with anhidrosis (CIPA) Congenital pulmonary airway malformation (CPAM) Conjoined twins; Costello syndrome; Craniopagus ...
Life Goes On: First major character with Down syndrome on a television series, portrayed by a person who also has Down syndrome. Chris Burke [113] 2018 Penny Stevenson: Doctors: She was born with a right arm that ends just below the elbow. Cerrie Burnell [114] 1994 Kerry Weaver: ER: Limp in her gait due to congenital hip dysplasia: Laura Innes ...
All patients with mirrored-self misidentification have some type of right hemisphere dysfunction. [4] The right hemisphere, particularly frontal right hemisphere circuits, [7] is involved in processing self-related stimuli and helps one recognize a picture or reflection of oneself. [8]
Movement disorders are clinical syndromes with either an excess of movement or a paucity of voluntary and involuntary movements, unrelated to weakness or spasticity. [1] Movement disorders present with extrapyramidal symptoms and are caused by basal ganglia disease . [ 2 ]
Walker–Warburg syndrome (WWS), also called Warburg syndrome, Chemke syndrome, HARD syndrome (Hydrocephalus, Agyria and Retinal Dysplasia), Pagon syndrome, cerebroocular dysgenesis (COD) or cerebroocular dysplasia-muscular dystrophy syndrome (COD-MD), [1] is a rare form of autosomal recessive congenital muscular dystrophy. [2]
Situs inversus (also called situs transversus or oppositus) is a congenital condition in which the major visceral organs are reversed or mirrored from their normal positions. . The normal arrangement of internal organs is known as situs solit