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ICD 10NA Congenital malformation
Q00 Q00 Anencephaly and similar malformationAnencephaly and similar malformation
Q01Q01 EncephaloceleEncephalocele
Q02Q02 MicrocephalyMicrocephaly
Q03Q03 Congenital hydrocephalusCongenital hydrocephalus
Q04Q04 Other congenital malformations of brainOther congenital malformations of brain
Q05Q05 Spina bifidaSpina bifida
Q06Q06 Other congenital malformations of spinal cordOther congenital malformations of spinal cord
Q07Q07 Other congenital malformations of nervous systemOther congenital malformations of nervous system
Q04.6Congenital cerebral cysts
Q04.60 PorencephalyQ04.60 Porencephaly
Q04.61 SchizencephalyQ04.61 Schizencephaly
Q04.62 Multicystic encephalomalaciaQ04.62 Multicystic encephalomalacia
Q04.63 Congenital leptomeningeal cystQ04.63 Congenital leptomeningeal cyst
Schizencephaly
Q02Microcephaly
Q02.-0 HydromicrocephalyQ02.-0 Hydromicrocephaly
Q02.-1 MicrencephalonQ02.-1 Micrencephalon
Q03Congenital hydrocephalus
Q03.0 Malformations of aqueduct of SylviusQ03.0 Malformations of aqueduct of Sylvius
Q03.1 Atresia of foramina of Magendie and Luschka Q03.1 Atresia of foramina of Magendie and Luschka (Dandy Walker Syndrome)(Dandy Walker Syndrome)
Q03.8 Other congenital hydrocephalusQ03.8 Other congenital hydrocephalus
Q03.80 Congenital hydrocephalus in malformations Q03.80 Congenital hydrocephalus in malformations classified elsewhereclassified elsewhere
Q03.9 Congenital hydrocephalus, unspecifiedQ03.9 Congenital hydrocephalus, unspecified
Q04Other congenital malformations of brain Q04.0Congenital malformations of corpus callosumQ04.0Congenital malformations of corpus callosum
Q04.00Total agenesis of corpus callosumQ04.00Total agenesis of corpus callosum Q04.01Partial agenesis of corpus callosumQ04.01Partial agenesis of corpus callosum 04.02Agenesis with lipoma of corpus callosum04.02Agenesis with lipoma of corpus callosum 04.08Other congenital malformation of corpus 04.08Other congenital malformation of corpus
callosumcallosum
Q04.1ArhinencephalyQ04.1Arhinencephaly
Q04.2HoloprosencephalyQ04.2Holoprosencephaly
Holoporencepahly
Lobar Holoprosencepaly
Q04Other congenital malformations of brain Q04.4Septo-optic dysplasiaQ04.4Septo-optic dysplasia
Q04.5 MegalencephalyQ04.5 Megalencephaly
Q04.50 Symmetrical megalencephalyQ04.50 Symmetrical megalencephaly
Q04.6Congenital cerebral cystsQ04.6Congenital cerebral cysts
Q04.60PorencephalyQ04.60Porencephaly
Q04.61SchizencephalyQ04.61Schizencephaly
Q04.62Multicystic encephalomalaciaQ04.62Multicystic encephalomalacia
Q04.63Congenital leptomeningeal cystQ04.63Congenital leptomeningeal cyst
Septo-optic Dysplasia (de Morsier Syndrome)
Clinical History:Clinical History: The patient has nystagmus and diminished visual The patient has nystagmus and diminished visual acuity. acuity.
Findings: Findings: The axial flair image as well as the coronal T1 weighted The axial flair image as well as the coronal T1 weighted MR image demonstrate absence of the septum pellucidum. The MR image demonstrate absence of the septum pellucidum. The coronal T1 weighted image also demonstrates hypoplasia of the coronal T1 weighted image also demonstrates hypoplasia of the optic chiasm. The coronal T2 weighted image demonstrates optic chiasm. The coronal T2 weighted image demonstrates hypoplastic optic nerveshypoplastic optic nerves
Hemimegalencephaly