Aicardi Syndrome
PR: 0
Aicardi Syndrome - This is a rare genetic condition characterised by: aicardi syndrome, genetic, genes, cleft lip, cleft lip and palate, malformation, retinal detachment, microphthalmia, short, growth retardation, hypotonia, rare, mental retardation, microcephaly, nystagmus, optic atrophy, precocious puberty, x linked dominant, facial asymmetry, inherited diseases |
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Aicardi Syndrome
PR: 0
Aicardi Syndrome - This is a rare genetic condition characterised by: aicardi syndrome, genetic, genes, cleft lip, cleft lip and palate, malformation, retinal detachment, microphthalmia, short, growth retardation, hypotonia, rare, mental retardation, microcephaly, nystagmus, optic atrophy, precocious puberty, x linked dominant, facial asymmetry, inherited diseases |
Orthostatic Intolerance Syndromes
PR: 0
NDRF provides patient support, medical referral, educational material, newsletters, an online discussion forum and a research protocol database for individuals impacted with dysautonomia. Dysautonomia, Autonomic Disorders, Orthostatic Intolerance, Postural Orthostatic Intolerance, POTS, OI, MVP Syndrome, MVP Dysautonomia, Mitral Valve Prolapse Syndrome, Orthostatic Hypotension, Low Blood Pressure, Syncope, Feinting, Autonomic, Autonomic Nervous System, PAF, Pure Autonomic Failure, MSA, Multiple System Atrophy, Shy-Drager Syndrome, Shy Drager, GBS, Autonomic Nervous System, Neurally Mediated Syncope, Neurocardiogenic Syncope, Chronic Orthostatic Intolerance, COI, Idiopathic Hypovolemia, Idiopathic Hypotension, Norepinephrine, Catecholamine, Catecholamine Disorders, Baroreflex Failure, Pheochromocytoma, Neuroblastoma, Chemodectoma, Familial Dysautonomia, Autonomic Neuropathies, Chagas Disease, Fludrocortisone, Midodrine, Erythropoietin |
Aicardi Syndrome
PR: 0
Aicardi Syndrome - This is a rare genetic condition characterised by: aicardi syndrome, genetic, genes, cleft lip, cleft lip and palate, malformation, retinal detachment, microphthalmia, short, growth retardation, hypotonia, rare, mental retardation, microcephaly, nystagmus, optic atrophy, precocious puberty, x linked dominant, facial asymmetry, inherited diseases |