Informaţii despre

Nume Porencephaly
Pagina Web www.malacards.org
Clasificare globală Malacards Boli fetale; Boli genetice; Boli rare
Clasificari ICD10 Congenital cerebral cysts
Clasificare anatomică Malacards Boli neuronale
Boli din aceeaşi familie Acquired Porencephaly; Familial Porencephaly; Porencephaly 1; Porencephaly 2

Vezi şi

Boli A-Z Absence of Septum Pellucidum Acquired Porencephaly Acute Liver Failure Afibrinogenemia Aging Alacrima, Achalasia, and Mental Retardation Syndrome Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Al-Raqad Syndrome Amaurosis Fugax Anencephaly Aneurysm Angiopathy, Hereditary, with Nephropathy, Aneurysms, and Muscle Cramps Aniridia 1 Anorexia Nervosa 1 Antiphospholipid Syndrome Antithrombin Iii Deficiency Aortic Aneurysm Arachnoid Cysts Arachnoiditis Arteritic Anterior Ischemic Optic Neuropathy Arthrochalasia Ehlers-Danlos Syndrome Bamforth Syndrome Baraitser-Winter Syndrome 1 Behr Syndrome Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen Blood Group, I System Blood Protein Disease Budd-Chiari Syndrome Buerger Disease Cataract Catastrophic Antiphospholipid Syndrome Central Retinal Vein Occlusion Cephalic Disorders Cerebellar Hypoplasia Cerebral Hemorrhage Cerebral Palsy Cerebral Sinovenous Thrombosis Cerebritis Cerebrovascular Disease Choroiditis Corneal Dystrophy, Posterior Polymorphous, 3 Cryptogenic Cirrhosis Cutis Marmorata Telangiectatica Congenita Cytomegalic Inclusion Disease Cytomegalovirus Infection Disseminated Intravascular Coagulation Dysfibrinogenemia Encephalitis Encephalocele Encephalomalacia Encephalopathy Epilepsy Factor V Deficiency Factor Viii Deficiency Factor X Deficiency Familial Porencephaly Fanconi Anemia, Complementation Group E Fibromatosis Glycogen Storage Disease Vi Hellp Syndrome Hemiplegia Hemoglobin E Disease Hemorrhage, Intracerebral Hepatic Infarction Homocysteinemia Homocystinuria Hydranencephaly Hydrocephalus Hydronephrosis Hypertelorism Hypotonia Inferior Vena Cava Interruption Intracranial Hypertension Intracranial Thrombosis Ischemic Colitis Ischemic Neuropathy Ischemic Optic Neuropathy Livedoid Vasculopathy Marantic Endocarditis Meningitis Mesenteric Vascular Occlusion Microcephaly Myoclonus Neonatal Meningitis Nevus, Epidermal Nonarteritic Anterior Ischemic Optic Neuropathy Orofaciodigital Syndrome Paracetamol Poisoning Patent Foramen Ovale Peripheral Vertigo Placental Abruption Polycystic Liver Disease 1 Polymicrogyria Porencephaly, Cerebellar Hypoplasia, and Internal Malformations Portal Vein Thrombosis Post-Thrombotic Syndrome Pregnancy Loss, Recurrent 1 Protein C Deficiency Protein S Deficiency Prothrombin Deficiency Prothrombin Deficiency, Congenital Pulmonary Embolism Purpura Renal Hypoplasia Retinal Artery Occlusion Retinal Vascular Occlusion Retinal Vein Occlusion Retinitis Sagittal Sinus Thrombosis Schizencephaly Scott Syndrome Sinusitis Sneddon Syndrome Spastic Cerebral Palsy Spastic Hemiplegia Spasticity Spinal Cord Infarction Strabismus Stroke, Ischemic Sudden Sensorineural Hearing Loss Thrombasthenia Thrombocytopenia Thrombophilia Thrombophilia Due to Activated Protein C Resistance Thrombophilia Due to Thrombin Defect Thrombophlebitis Thrombosis Varicose Veins Vein Disease Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 Von Willebrand's Disease West Syndrome