sturge weber mnemonic

Am J Med Genet. [2] It is characterized as a part of the neuroectodermal dysplasias, also known as phakomatoses. USMLE Mnemonics. doi: 10.1002/ajmg.1320570110 . OTHER SETS BY THIS CREATOR. 0 1. 1995; 57 (1): p.35-45. N/A. Browse. 10 terms. Sturge-Weber Syndrome. PortWine stain Guthrie card: diseases identified with it "Guthrie Cards Can Help Predict Bad Metabolism": Galactosaemia Cystic fibrosis Congenital adrenal hyperplasia Hypothyroidism Phenylketonuria Biotidinase deficiency Maple syrup urine disease Croup: symptoms 3 S's: Stridor 58 terms. Sturge-Weber Syndrome (SWS), also known as encephalotrigeminal angiomatosis, is a congenital neuro-oculocutaneous syndrome that presents at birth. Moises Dominguez 0 % Topic. 51 terms. Sturge-Weber Syndrome (SWS) (encephelotrigeminal angiomatosis) is a congenital, non-familial disorder caused by the GNAQ gene mutation. GNAQ gene codes for a Gq protein that is associated with G-protein coupled receptors and can activate phospholipase C. 0. Learn vocabulary, terms, and more with flashcards, games, and other study tools. Seizures 2. ... USMLE step 1 - mnemonics. It is characterized by a … Sturge Weber syndrome, sometimes called encephalotrigeminal angiomatosis, is a rare congenital neurocutaneous disorder characterized by proliferation of arteries in the brain resulting in multiple angiomas. [1] SWS was first reported by Dr. Schirmer in 1860 with later descriptions by Dr. Sturge in 1897 and Dr. Weber in 1922. 0. 97 terms. PortWine stain Guthrie card: diseases identified with it "Guthrie Cards Can Help Predict Bad Metabolism": Galactosaemia Cystic fibrosis Congenital adrenal hyperplasia Hypothyroidism Phenylketonuria Biotidinase deficiency Maple syrup urine disease Croup: symptoms 3 S's: Stridor Sturge Weber Syndrome - STURGE. Questions. 0. | Open in Read by QxMD; Day AM, McCulloch CE, Hammill AM, et al. Physical and Family History Variables Associated With Neurological and Cognitive Development in Sturge-Weber Syndrome. Start studying USMLE Mnemonics 3. sunshinesweetheart outcomes: stork bite/salmon patch will regress by 5-6year old or persist into adulthood; strawberry hemangioma will regress by 3-6 year old; port wine stain will regress or persist but it'll be associated with the sturge-weber stuff see the mnemonic pg 513 of FA 2019) + Sturge-Weber syndrome: hallmark features Sturge-Weber: 1. A genetic somatic activating mutation in the GNAQ gene during fetal development has been found to cause both port wine stains (a common congenital malformation) and the Sturge Weber Syndrome. Review Topic. Mnemonics. Search. 58 terms. Sturge-Weber syndrome: hallmark features Sturge-Weber: 1. N/A. Medical Mnemonics - Sturge-Weber Syndrome: Hallmark Features - Pediatrics Mnemonics - Study for your IM Boards using the Knowmedge Internal Medicine medical mnemonics. USMLE Mnemonics. Seizures 2. Specifically, patients demonstrate leptomeningeal angiomas and … Snapshot: A 5-year-old male presents with an un provoked convulsive episode that lead to right-sided hemiparesis. 0. Sturge-Weber syndrome (SWS) is a neurological disorder marked by a distinctive port-wine stain on the forehead, scalp, or around the eye. Step 2 DDX Workup. Sporadic port wine Stain Tram track calcifications Unilateral Retardation Glaucoma GNAQ gene (activating mutation) Epilepsy. Sujansky E, Conradi S. Outcome of Sturge-Weber syndrome in 52 adults. Tram track calcifications Unilateral Retardation Glaucoma GNAQ gene ( activating mutation ).... For your IM Boards using the Knowmedge Internal Medicine medical Mnemonics - Study for your Boards! Associated with Neurological and Cognitive Development in Sturge-Weber Syndrome ( SWS ) ( encephelotrigeminal )! ) is a congenital, non-familial disorder caused by the GNAQ gene mutation Neurological and Cognitive Development Sturge-Weber... 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