Acrocallosal Syndrome

Known as: Hallux Duplication, Postaxial Polydactyly, and Absence of Corpus Callosum, Acrocallosal Syndrome [Disease/Finding], Syndrome, Acrocallosal 
Autosomal recessive syndrome characterized by hypogenesis or agenesis of CORPUS CALLOSUM. Clinical features include MENTAL RETARDATION; CRANIOFACIAL… (More)
National Institutes of Health

Papers overview

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Highly Cited
2011
Highly Cited
2011
KIF7, the human ortholog of Drosophila Costal2, is a key component of the Hedgehog signaling pathway. Here we report mutations in… (More)
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2009
2009
To evaluate proprioceptive potential in residual remnants, tissue harvested from ruptured ACLs in 63 consecutive patients was… (More)
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2003
2003
Greig cephalopolysyndactyly syndrome (GCPS) is caused by haploinsufficiency of GLI3 on 7p13. Features of GCPS include polydactyly… (More)
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2002
2002
Acrocallosal syndrome (ACS) is an autosomal recessive condition, characterized by agenesis of the corpus callosum, pre- and… (More)
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Highly Cited
2002
Highly Cited
2002
PURPOSE This study presents the 2- to 10-year results of 35 arthroscopically assisted combined anterior cruciate ligament and… (More)
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1990
1990
A 6 month old Turkish boy with the acrocallosal syndrome is reported. The patient, born to consanguineous, healthy parents… (More)
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Review
1989
Review
1989
The acrocallosal syndrome (ACS) is a probable autosomal recessive condition of macrocephaly, craniofacial and hand and foot… (More)
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1989
1989
We describe a 21-month-old girl with typical manifestations of the acrocallosal syndrome of craniofacial anomalies, agenesis of… (More)
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1988
1988
The acrocallosal syndrome is characterized by peculiar facies, polydactyly of the hands and/or feet, and agenesis of the corpus… (More)
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1986
1986
Two sisters born to non-consanguineous healthy parents are described who present the following abnormalities: macrocephalus… (More)
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