serw-MX  [xml]  

 DeCS Categories

C04 Neoplasms .
C04.588 Neoplasms by Site .
C04.588.322 Endocrine Gland Neoplasms .
C04.588.322.455 Ovarian Neoplasms .
C04.588.322.455.531 Meigs Syndrome .
C05 Musculoskeletal Diseases .
C05.116 Bone Diseases .
C05.116.099 Bone Diseases, Developmental .
C05.116.099.674 Marfan Syndrome .
C05.651 Muscular Diseases .
C05.651.460 Mitochondrial Myopathies .
C05.651.460.620 Mitochondrial Encephalomyopathies .
C05.651.460.620.520 MELAS Syndrome .
C10 Nervous System Diseases .
C10.228 Central Nervous System Diseases .
C10.228.140 Brain Diseases .
C10.228.140.079 Basal Ganglia Diseases .
C10. Meige Syndrome .
C10.228.140.163 Brain Diseases, Metabolic .
C10. Brain Diseases, Metabolic, Inborn .
C10. Leigh Disease .
C10. MELAS Syndrome .
C10.228.140.300 Cerebrovascular Disorders .
C10.228.140.300.275 Cerebral Small Vessel Diseases .
C10.228.140.300.275.500 MELAS Syndrome .
C10.228.662 Movement Disorders .
C10.228.662.300 Dystonic Disorders .
C10.228.662.300.500 Meige Syndrome .
C10.668 Neuromuscular Diseases .
C10.668.491 Muscular Diseases .
C10.668.491.500 Mitochondrial Myopathies .
C10.668.491.500.500 Mitochondrial Encephalomyopathies .
C10.668.491.500.500.500 MELAS Syndrome .
C13 Female Urogenital Diseases and Pregnancy Complications .
C13.351 Female Urogenital Diseases .
C13.351.500 Genital Diseases, Female .
C13.351.500.056 Adnexal Diseases .
C13.351.500.056.630 Ovarian Diseases .
C13.351.500.056.630.705 Ovarian Neoplasms .
C13.351.500.056.630.705.531 Meigs Syndrome .
C13.351.937 Urogenital Neoplasms .
C13.351.937.418 Genital Neoplasms, Female .
C13.351.937.418.685 Ovarian Neoplasms .
C13.351.937.418.685.531 Meigs Syndrome .
C14 Cardiovascular Diseases .
C14.240 Cardiovascular Abnormalities .
C14.240.400 Heart Defects, Congenital .
C14.240.400.725 Marfan Syndrome .
C14.280 Heart Diseases .
C14.280.400 Heart Defects, Congenital .
C14.280.400.725 Marfan Syndrome .
C14.907 Vascular Diseases .
C14.907.253 Cerebrovascular Disorders .
C14.907.253.329 Cerebral Small Vessel Diseases .
C14.907.253.329.500 MELAS Syndrome .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.131 Congenital Abnormalities .
C16.131.077 Abnormalities, Multiple .
C16.131.077.550 Marfan Syndrome .
C16.131.240 Cardiovascular Abnormalities .
C16.131.240.400 Heart Defects, Congenital .
C16.131.240.400.720 Marfan Syndrome .
C16.320 Genetic Diseases, Inborn .
C16.320.540 Marfan Syndrome .
C16.320.565 Metabolism, Inborn Errors .
C16.320.565.189 Brain Diseases, Metabolic, Inborn .
C16.320.565.189.412 Leigh Disease .
C16.320.565.189.535 MELAS Syndrome .
C16.320.565.202 Carbohydrate Metabolism, Inborn Errors .
C16.320.565.202.810 Pyruvate Metabolism, Inborn Errors .
C16.320.565.202.810.444 Leigh Disease .
C17 Skin and Connective Tissue Diseases .
C17.300 Connective Tissue Diseases .
C17.300.500 Marfan Syndrome .
C18 Nutritional and Metabolic Diseases .
C18.452 Metabolic Diseases .
C18.452.132 Brain Diseases, Metabolic .
C18.452.132.100 Brain Diseases, Metabolic, Inborn .
C18.452.132.100.412 Leigh Disease .
C18.452.132.100.535 MELAS Syndrome .
C18.452.648 Metabolism, Inborn Errors .
C18.452.648.189 Brain Diseases, Metabolic, Inborn .
C18.452.648.189.412 Leigh Disease .
C18.452.648.189.535 MELAS Syndrome .
C18.452.648.202 Carbohydrate Metabolism, Inborn Errors .
C18.452.648.202.810 Pyruvate Metabolism, Inborn Errors .
C18.452.648.202.810.444 Leigh Disease .
C18.452.660 Mitochondrial Diseases .
C18.452.660.520 Leigh Disease .
C18.452.660.560 Mitochondrial Myopathies .
C18.452.660.560.620 Mitochondrial Encephalomyopathies .
C18.452.660.560.620.520 MELAS Syndrome .
C19 Endocrine System Diseases .
C19.344 Endocrine Gland Neoplasms .
C19.344.410 Ovarian Neoplasms .
C19.344.410.531 Meigs Syndrome .
C19.391 Gonadal Disorders .
C19.391.630 Ovarian Diseases .
C19.391.630.705 Ovarian Neoplasms .
C19.391.630.705.531 Meigs Syndrome .
C23 Pathological Conditions, Signs and Symptoms .
C23.550 Pathologic Processes .
C23.550.288 Disease .
C23.550.288.500 Syndrome .
 Synonyms & Historicals
Meige Syndrome .
Blepharospasm-Oromandibular Dyskinesia .
Blepharospasm-Oromandibular Dystonia Syndrome .
Blepharospasm-Oromandibular Dystonia Syndrome, Idiopathic .
Idiopathic Blepharospasm-Oromandibular Dystonia Syndrome .
Syndrome, Blepharospasm-Oromandibular Dystonia .
Blepharospasm Oromandibular Dyskinesia .
Blepharospasm Oromandibular Dystonia .
Blepharospasm Oromandibular Dystonia Syndrome .
Blepharospasm Oromandibular Dystonia Syndrome, Idiopathic .
Blepharospasm-Oromandibular Dyskinesias .
Blepharospasm-Oromandibular Dystonia Syndromes .
Blepharospasm-Oromandibular Dystonias .
Dyskinesia, Blepharospasm-Oromandibular .
Dyskinesia, Idiopathic Orofacial .
Dyskinesias, Blepharospasm-Oromandibular .
Dyskinesias, Idiopathic Orofacial .
Dystonia Syndrome, Blepharospasm-Oromandibular .
Dystonia Syndromes, Blepharospasm-Oromandibular .
Dystonia, Blepharospasm-Oromandibular .
Dystonias, Blepharospasm-Oromandibular .
Idiopathic Blepharospasm Oromandibular Dystonia Syndrome .
Idiopathic Orofacial Dyskinesias .
Orofacial Dyskinesia, Idiopathic .
Orofacial Dyskinesias, Idiopathic .
Blepharospasm-Oromandibular Dystonia .
Brueghel Syndrome .
Idiopathic Orofacial Dyskinesia .
A syndrome characterized by orofacial DYSTONIA; including BLEPHAROSPASM; forceful jaw opening; lip retraction; platysma muscle spasm; and tongue protrusion. It primarily affects older adults, with an incidence peak in the seventh decade of life. (From Adams et al., Principles of Neurology, 6th ed, p108) .
Meigs Syndrome .
Meigs' Syndrome .
Meig Syndrome .
Meig's Syndrome .
The triad of benign FIBROMA or other ovarian tumors with ASCITES, and HYDROTHORAX due to large PLEURAL EFFUSIONS. .
Syndrome .
Symptom Cluster .
Cluster, Symptom .
Clusters, Symptom .
Symptom Clusters .
Syndromes .
A characteristic symptom complex. .
MELAS Syndrome .
Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-Like Episodes .
Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, And Stroke-Like Episodes .
Myopathy, Mitochondrial-Encephalopathy-Lactic Acidosis-Stroke .
Syndrome, MELAS .
Mitochondrial Myopathy, Lactic Acidosis, Stroke-Like Episode .
A mitochondrial disorder characterized by focal or generalized seizures, episodes of transient or persistent neurologic dysfunction resembling strokes, and ragged-red fibers on muscle biopsy. Affected individuals tend to be normal at birth through early childhood, then experience growth failure, episodic vomiting, and recurrent cerebral insults resulting in visual loss and hemiparesis. The cortical lesions tend to occur in the parietal and occipital lobes and are not associated with vascular occlusion. VASCULAR HEADACHE is frequently associated and the disorder tends to be familial. (From Joynt, Clinical Neurology, 1992, Ch56, p117) .
Leigh Disease .
Encephalomyelopathy, Subacute Necrotizing .
Encephalopathy, Subacute Necrotizing, Infantile .
Encephalopathy, Subacute Necrotizing, Juvenile .
Infantile Leigh Disease .
Infantile Subacute Necrotizing Encephalopathy .
Juvenile Leigh Disease .
Juvenile Subacute Necrotizing Encephalopathy .
Leigh Disease, Infantile .
Leigh Disease, Juvenile .
Leigh Syndrome .
Leigh's Disease .
Subacute Necrotizing Encephalomyelitis, Infantile .
Subacute Necrotizing Encephalomyelopathy .
Subacute Necrotizing Encephalopathy .
Subacute Necrotizing Encephalopathy, Infantile .
Subacute Necrotizing Encephalopathy, Juvenile .
Disease, Leigh's .
Encephalomyelitides, Subacute Necrotizing .
Encephalomyelopathies, Subacute Necrotizing .
Encephalopathies, Subacute Necrotizing .
Leighs Disease .
Necrotizing Encephalomyelitides, Subacute .
Necrotizing Encephalomyelitis, Subacute .
Necrotizing Encephalomyelopathies, Subacute .
Necrotizing Encephalomyelopathy, Subacute .
Necrotizing Encephalopathies, Subacute .
Necrotizing Encephalopathy, Subacute .
Subacute Necrotizing Encephalomyelitides .
Subacute Necrotizing Encephalomyelitis .
Subacute Necrotizing Encephalomyelopathies .
Subacute Necrotizing Encephalopathies .
Encephalomyelitis, Subacute Necrotizing .
Encephalopathy, Subacute Necrotizing .
A group of metabolic disorders primarily of infancy characterized by the subacute onset of psychomotor retardation, hypotonia, ataxia, weakness, vision loss, eye movement abnormalities, seizures, dysphagia, and lactic acidosis. Pathological features include spongy degeneration of the neuropile of the basal ganglia, thalamus, brain stem, and spinal cord. Patterns of inheritance include X-linked recessive, autosomal recessive, and mitochondrial. Leigh disease has been associated with mutations in genes for the PYRUVATE DEHYDROGENASE COMPLEX; CYTOCHROME-C OXIDASE; ATP synthase subunit 6; and subunits of mitochondrial complex I. (From Menkes, Textbook of Child Neurology, 5th ed, p850). .
Marfan Syndrome .
Marfan Syndrome, Type I .
Marfan's Syndrome .
Marfans Syndrome .
Syndrome, Marfan .
Syndrome, Marfan's .
An autosomal dominant disorder of CONNECTIVE TISSUE with abnormal features in the heart, the eye, and the skeleton. Cardiovascular manifestations include MITRAL VALVE PROLAPSE, dilation of the AORTA, and aortic dissection. Other features include lens displacement (ectopia lentis), disproportioned long limbs and enlarged DURA MATER (dural ectasia). Marfan syndrome is associated with mutations in the gene encoding fibrillin, a major element of extracellular microfibrils of connective tissue. .