Acrocallosal syndrome: Difference between revisions
(New page: {{Infobox_Disease | Name = {{PAGENAME}} | Image = | Caption = | DiseasesDB = | ICD10 = | ICD9 = | ICDO = | OMIM ...) |
No edit summary |
||
Line 13: | Line 13: | ||
MeshID = D055673 | | MeshID = D055673 | | ||
}} | }} | ||
{{SI}} | |||
{{CMG}} | |||
{{EH}} | |||
'''Acrocallosal syndrome''' (also known as '''ACLS''') is a rare [[autosomal]] [[recessive]] syndrome characterized by [[corpus callosum agenesis]], [[polydactyly]], multiple [[dysmorphic feature]]s, motor and mental retardation, and other symptoms.<ref>{{OMIM|200990|Acrocallosal syndrome; ACLS}}</ref> The syndrome was first described by Albert Schinzel in 1979.<ref>{{cite journal |first=Albert |last=Schinzel |title=Postaxial polydactyly, hallux duplication, absence of the corpus callosum, macroencephaly and severe mental retardation: a new syndrome? |journal=Helvetica Paediatrica Acta |volume=34 |issue=2 |pages=141–6 |year=1979 |month=May |pmid=457430 |doi= |url=http://www.ncbi.nlm.nih.gov/pubmed/457430?dopt=Abstract}}</ref> | '''Acrocallosal syndrome''' (also known as '''ACLS''') is a rare [[autosomal]] [[recessive]] syndrome characterized by [[corpus callosum agenesis]], [[polydactyly]], multiple [[dysmorphic feature]]s, motor and mental retardation, and other symptoms.<ref>{{OMIM|200990|Acrocallosal syndrome; ACLS}}</ref> The syndrome was first described by Albert Schinzel in 1979.<ref>{{cite journal |first=Albert |last=Schinzel |title=Postaxial polydactyly, hallux duplication, absence of the corpus callosum, macroencephaly and severe mental retardation: a new syndrome? |journal=Helvetica Paediatrica Acta |volume=34 |issue=2 |pages=141–6 |year=1979 |month=May |pmid=457430 |doi= |url=http://www.ncbi.nlm.nih.gov/pubmed/457430?dopt=Abstract}}</ref> | ||
Revision as of 21:06, 12 April 2009
Acrocallosal syndrome | |
OMIM | 200990 |
---|---|
MeSH | D055673 |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Please Take Over This Page and Apply to be Editor-In-Chief for this topic: There can be one or more than one Editor-In-Chief. You may also apply to be an Associate Editor-In-Chief of one of the subtopics below. Please mail us [2] to indicate your interest in serving either as an Editor-In-Chief of the entire topic or as an Associate Editor-In-Chief for a subtopic. Please be sure to attach your CV and or biographical sketch.
Acrocallosal syndrome (also known as ACLS) is a rare autosomal recessive syndrome characterized by corpus callosum agenesis, polydactyly, multiple dysmorphic features, motor and mental retardation, and other symptoms.[1] The syndrome was first described by Albert Schinzel in 1979.[2]
References
- ↑ Online Mendelian Inheritance in Man (OMIM) Acrocallosal syndrome; ACLS -200990
- ↑ Schinzel, Albert (1979). "Postaxial polydactyly, hallux duplication, absence of the corpus callosum, macroencephaly and severe mental retardation: a new syndrome?". Helvetica Paediatrica Acta. 34 (2): 141–6. PMID 457430. Unknown parameter
|month=
ignored (help)
External links
Template:Congenital malformations and deformations of nervous system