Marfan syndrome: Difference between revisions

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 {{ICD10 transition status
-| OldDxArticle =| CurrentStatus = freshly automatically generated article
+| OldDxArticle = Marfan Syndrome
-| InitialEditorAssigned = Shirley Kiesman
+| CurrentStatus = reconciled
-| MinimumCombinedCodes =
+| InitialEditorAssigned = not assigned
 }}
 {{ICD10 dx
+| MinimumCombinedCodes =
 | ICD10 Code=Q87.4
-| BugRequired= required
+| BugRequired=
 }}
+{{ICD10 category|Cardiovascular}}{{ICD10 category|Hereditary/congenital}}
 == Additional Info ==
+[https://en.wikipedia.org/wiki/Marfan_syndrome Marfan syndrome on wikipedia]
+*Marfan syndrome (or Marfan's syndrome) is a genetic disorder of the connective tissue.
+*People with Marfan's are typically tall, with long limbs and long thin fingers.
-== Alternate ICD10s to consider coding instead ==
+*The most serious complication is defects of the heart valves and aorta. It may also affect the lungs, eyes, the dural sac surrounding the spinal cord, skeleton and the hard palate.
-(turn these into links to the actual diagnosis articles if possible. For some that might make no sense.)
+== Alternate ICD10s to consider coding instead or in addition ==
 == Candidate [[Combined ICD10 codes]] ==
-(put links to likely candidates coded with this one, eg. a cause for a trauma.)
+*[[Mitral valve prolapse]]
+*[[Aortic aneurysm, NOS with rupture]]
+*[[Aortic aneurysm, NOS without mention of rupture]]
+*[[Aortic aneurysm, thoracic without mention of rupture]]
+*[[Aortic aneurysm, thoracic with rupture]]
+== Related CCI Codes ==
+{{Data Integrity Check List}}
 == Related Articles ==
 {{Related Articles}}
+{{ICD10 footer}}
+{{EndPlaceHolder}}