Skip to search formSkip to main contentSkip to account menu

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… 
National Institutes of Health

Related topics

Related topics

35 relations
ACLS geneAccessory tragusAnus, ImperforateAutosomal recessive inheritance

Narrower (1)

Acrocallosal syndrome, Schinzel type

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2014
2014
Meniscus Injuries Alter the Kinematics of Knees With Anterior Cruciate Ligament Deficiency
Background: Most knee joint biomechanics studies have involved knees with an isolated anterior cruciate ligament (ACL) injury… 
2007
2007
Current Status of CPR in Korea
Cardiac Arrest victims are increasing but EMS is not ready for them, in Korea. At this time, we need to know the exact status… 
Highly Cited
1998
Highly Cited
1998
Effects of adding links to "the chain of survival" for prehospital cardiac arrest: a contrast in outcomes in 1975 and 1995 at a single institution.
Review
1997
Review
1997
Acrocallosal syndrome in an Algerian boy born to consanguineous parents: review of the literature and further delineation of the syndrome.
We present a 17-month-old boy with the acrocallosal syndrome. He was born to consanguineous parents. Abnormal findings included… 
Review
1996
Review
1996
Knee extension and flexion: MR delineation of normal and torn anterior cruciate ligaments.
OBJECTIVE Our goal was to assess the effect of joint position of semiflexed and extended knees in MR delineation of the anterior… 
Review
1996
Review
1996
Clinical and molecular cytogenetic observations in three cases of "trisomy 12p syndrome".
Two unpublished cases with partial tandem duplication of 12p and one previously published case were studied by fluorescence in… 
1992
1992
Acrocallosal syndrome in a child with de novo inverted tandem duplication of 12p11.2-p13.3.
Report on the child of normal unrelated parents presenting the typical features of acrocallosal syndrome (craniofacial dysmorphy… 
1989
1989
Acrocallosal syndrome: new findings.
We describe a 21-month-old girl with typical manifestations of the acrocallosal syndrome of craniofacial anomalies, agenesis of… 
Review
1989
Review
1989
Hypogenitalism in the acrocallosal syndrome.
We have studied a boy with acrocallosal syndrome and hypogenitalism. He was the offspring of double first cousins. He had unusual… 
1988
1988
The acrocallosal syndrome in first cousins: widening of the spectrum of clinical features and further support for autosomal recessive inheritance.
First cousins, related through their mothers, showed a pattern of craniofacial, brain, and limb anomalies consistent with the… 
By clicking accept or continuing to use the site, you agree to the terms outlined in our Privacy Policy (opens in a new tab), Terms of Service (opens in a new tab), and Dataset License (opens in a new tab)