- Agenesis of the corpus callosum
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Agenesis of the corpus callosum Classification and external resources OMIM 217990 DiseasesDB 29900 eMedicine radio/193 Agenesis of the corpus callosum (ACC) is a rare birth defect (congenital disorder) in which there is a complete or partial absence of the corpus callosum. Agenesis of the corpus callosum occurs when the corpus callosum, the band of white matter connecting the two hemispheres in the brain, fails to develop normally, typically during pregnancy. The development of the fibers which would otherwise form the corpus callosum become longitudinally oriented within each hemisphere and form structures called Probst bundles.
In addition to agenesis of the corpus callosum, other callosal disorders include hypogenesis (partial formation), dysgenesis (malformation) of the corpus callosum, and hypoplasia (underdevelopment) of the corpus callosum.[1]
Contents
Diagnosis
Callosal disorders can only be diagnosed through a brain scan.[2] They may be diagnosed through an MRI, CT scan, prenatal ultrasound, or prenatal MRI.[1]
Cause
Agenesis of the corpus callosum is caused by disruption to development of the fetal brain between the 3rd and 12th week of pregnancy.[2] In most cases, it is not possible to know what caused an individual to have ACC or another callosal disorder. However, research suggests that some possible causes may include chromosome errors, inherited genetic factors, prenatal infections or injuries, prenatal toxic exposures, structural blockage by cysts or other brain abnormalities, and metabolic disorders.[1]
Relation to other rare disorders: genetic ciliopathy
Until recently, the medical literature did not indicate a connection among many genetic disorders, both genetic syndromes and genetic diseases, that are now being found to be related. As a result of new genetic research, some of these are, in fact, highly related in their root cause despite the widely varying symptoms apparent on clinical examination. Agenesis of the corpus callosum is one such disease, part of an emerging class of diseases called ciliopathies. The underlying cause may be a dysfunctional molecular mechanism in the primary cilia structures of the cell organelles which are present in many cellular types throughout the human body. The cilia defects adversely affect "numerous critical developmental signaling pathways" essential to cellular development and thus offer a plausible hypothesis for the often multi-symptom nature of a large set of syndromes and diseases. Known ciliopathies include primary ciliary dyskinesia, Bardet-Biedl syndrome, polycystic kidney and liver disease, nephronophthisis, Alstrom syndrome, Meckel-Gruber syndrome and some forms of retinal degeneration.[3]
Signs and symptoms
Signs and symptoms of ACC and other callosal disorders vary greatly among individuals. However, some characteristics common in individuals with callosal disorders include vision impairments, low muscle tone (hypotonia), poor motor coordination, delays in motor milestones such as sitting and walking, low perception of pain, delayed toilet training, and chewing and swallowing difficulties. Laboratory research has demonstrated that individuals with ACC have difficulty transferring more complex information from one hemisphere to the other.[4] They also have been shown to have some cognitive disabilities (difficulty in complex problem solving) and social difficulties (missing subtle social cues), even when their Intelligence Quotient is normal.[4] Recent research suggests that specific social difficulties may be a result of impaired face processing.[5] The unusual social behavior in childhood is often mistaken for or misdiagnosed as Asperger syndrome or other autism spectrum disorders. Other characteristics sometimes associated with callosal disorders include seizures, spasticity, early feeding difficulties and/or gastric reflux, hearing impairments, abnormal head and facial features, and mental retardation.[1]
Associated syndromes and conditions
Some syndromes that frequently include ACC are Aicardi syndrome, Andermann syndrome, Shapiro syndrome, acrocallosal syndrome, septo-optic dysplasia (optic nerve hypoplasia), Mowat-Wilson syndrome and Menkes syndrome. Some conditions that are sometimes associated with ACC include maternal nutritional deficiencies or infections, metabolic disorders, fetal alcohol syndrome, craniofacial abnormalities, and other oral and maxillofacial pathologies.[1]
Treatment
There are currently no specific medical treatments for callosal disorders, but individuals with ACC and other callosal disorders may benefit from a range of developmental therapies, educational support, and services. It is important to consult with a variety of medical, health, educational and social work professionals. Such professionals include neurologists, neuropsychologists, occupational therapists, physical therapists, speech and language pathologists, pediatricians, geneticists, special educators, early childhood intervention specialists, and caregivers for adults.[1]
Prognosis
Prognosis varies depending on the type of callosal abnormality and associated conditions or syndromes. It is not possible for the corpus callosum to regenerate (i.e. the corpus callosum will not regrow).[2] Neuropsychological testing reveals subtle differences in higher cortical function compared to individuals of the same age and education without ACC, although some individuals with callosal disorders have average intelligence and lead normal lives,
Notable cases
Kim Peek, inspiration for the film Rain Man and renowned for his savant abilities, was born with agenesis of the corpus callosum, along with macrocephaly and damage to the cerebellum.[6]
Notes
- ^ a b c d e f "ACC - What is agenesis of the corpus callosum?". University of Maine. http://www.umaine.edu/edhd/research/acc/what-is-agenesis-of-the-corpus-callosum-acc/. Retrieved April 11, 2010.
- ^ a b c "Corpus callosum disorders". National Organization for Disorders of the Corpus Callosum. https://www.nodcc.org/index.php?option=com_content&task=view&id=12&Itemid=27. Retrieved April 11, 2010.
- ^ Badano JL, Mitsuma N, Beales PL, Katsanis N (2006). "The Ciliopathies: An Emerging Class of Human Genetic Disorders". Annual Review of Genomics and Human Genetics 7: 125–148. doi:10.1146/annurev.genom.7.080505.115610. PMID 16722803. http://arjournals.annualreviews.org/doi/abs/10.1146/annurev.genom.7.080505.115610
- ^ a b "Agenesis of the Corpus Callosum". Travis Research Institute. http://www.travisinstitute.org/neuroscience/agenesis.htm. Retrieved April 11, 2010.
- ^ "Corpus Callosum Research Program". California Institute of Technology. http://emotion.caltech.edu/agcc/. Retrieved April 11, 2010.
- ^ Martin GN, Carlson NR, Buckist W (2007). Psychology (3rd ed.). London: Pearson Education Company.
External links
Support organizations:
- National Organization for Disorders of the Corpus Callosum Non - profit US organisation offering information and support.
- Corpal UK charity offering support to families caring for children with ACC.
- Agenesis of the Corpus Callosum Community A site with message boards for discussing ACC.
- ACC page from Contact a Family UK charity providing support and advice to families with disabled children or those with special needs.
- Aicardi Syndrome Foundation Support and information for families caring for children with Aicardi Syndrome.
- UCSF Fetal Treatment Center: Agenesis of the corpus callosum
- Caregiver Support and Personal Stories - Personal experiences of those affected by Agenesis of Corpus Callosum
Congenital malformations and deformations of nervous system (Q00–Q07, 740–742) Brain Anencephaly (Acephaly, Acrania, Acalvaria, Iniencephaly) · Encephalocele · Arnold–Chiari malformationOtherCNS cyst (Porencephaly, Schizencephaly)Spinal cord OtherCategories:- Congenital disorders of nervous system
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