Pontocerebellar hypoplasia
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Overview
Pontocerebellar hypoplasia (PCH) is a heterogeneous group of rare neurodegenerative disorders caused by genetic mutations and characterised by progressive atrophy of various parts of the brain such as the cerebellum or brainstem (particularly the pons).[1] Where known, these disorders are inherited in an autosomal recessive fashion. There is no known cure for PCH.[2]
Classification
Pontocerebellar hypoplasia is classified as follows:
| Type | OMIM | Gene | Locus | Distinctive features | Alternate names |
|---|---|---|---|---|---|
| PCH1A | 607596 | VRK1 | 14q32 | Infantile onset anterior horn cell degeneration resulting in progressive muscle atrophy; resembles infantile spinal muscular atrophy[3] | Spinal muscular atrophy with pontocerebellar hypoplasia (SMA-PCH) |
| PCH1B | 614678 | EXOSC3 | 9p13.2 | Cerebellar and spinal motor neuron degeneration beginning at birth and resulting in decreased body tone, respiratory insufficiency, muscle atrophy, progressive microcephaly and global developmental delay | |
| PCH2A | 277470 | TSEN54 | 17q25.1 | Dyskinetic movements, seizures (frequently) | Volendam neurodegenerative disease |
| PCH2B | 612389 | TSEN2 | 3p25.2 | ||
| PCH2C | 612390 | TSEN34 | 19q13.42 | ||
| PCH2D | 613811 | SEPSECS | 4p15.2 | Progressive cerebello-cerebral atrophy (PCCA) | |
| PCH2E | 615851 | VPS53 | 17p13.3 | Profound mental retardation, progressive microcephaly, spasticity, and early-onset epilepsy | |
| PCH3 | 608027 | CLAM | 7q11–q21 | Seizures, short stature, optic atrophy, progressive microcephaly, severe developmental delay; described only in a handful of cases.[4] | CLAM-PCH, cerebellar atrophy with progressive microcephaly |
| PCH4 | 225753 | TSEN54 | 17q25.1 | Severe prenatal form of PCH2 with excess fluid in the amniotic sac, muscle contractures, brief involuntary muscle twitching, brief episodes without breathing, and early death following birth | |
| PCH5 | 610204 | unknown | unknown | Severe prenatal form, described in one family | Olivopontocerebellar hypoplasia (OPCH) |
| PCH6 | 611523 | RARS2 | 6q15 | Severe encephalopathy in the newborn with hypotonia, and inconstantly: intractable seizures, edema, increased lactate blood levels, mitochondrial respiratory chain defects | |
| PCH7 | 614969 | unknown | unknown | Hypotonia, apneic episodes, seizures, vanishing testis[5][6] | |
| PCH8 | 614961 | CHMP1A | 16q24.3 | Severe psychomotor retardation, abnormal movements, hypotonia, spasticity, and variable visual defects | |
| PCH9 | 615809 | AMPD2 | 1p13.3 | Severely delayed psychomotor development, progressive microcephaly, spasticity, seizures, and brain abnormalities, including brain atrophy, thin corpus callosum, and delayed myelination[7] | |
| PCH10 | 615803 | CLP1 | 11q12.1 | Severely delayed psychomotor development, progressive microcephaly, spasticity, seizures, and brain abnormalities, including brain atrophy and delayed myelination |
Pontine and cerebellar hypoplasia is also observed in certain phenotypes of X-linked mental retardation (so called MICPCH, OMIM: 300749).
Signs and symptoms
There are different signs and symptoms for different forms of pontocerebellar hypoplasia, at least six of which have been described by researchers. All forms involve abnormal development of the brain, leading to slow development, movement problems, and intellectual impairment.[2]
The following values seem to be aberrant in children with CASK gene defects: lactate, pyruvate, 2-ketoglutaric acid, adipic acid, and suberic acid which seems to support the thesis that CASK affects mitochondrial function.[8]
Causes
Pontocerebellar hypoplasia is caused by mutations in genes including VRK1 (PCH1); TSEN2, TSEN34 (PCH2); RARS2 (PCH6); and TSEN54 (PCH2 and PCH4). The genes associated with PCH3 and PCH5 have not yet been identified.[2]
The mutated genes in PCH are autosomal recessive, which means that parents of an affected child each carry only one copy of the damaged gene. In each parent the other copy performs its proper function and they display no signs of PCH. A child inheriting two damaged copies of the gene will be affected by PCH.[2]
Mechanism
Mutations in the genes that cause PCH produce faults in the production of chemicals, usually enzymes, that are required for the development of nerve cells (neurons) and for properly processing RNA, which is needed for any cell to function normally. The exact mechanism by which PCH affects the development of the cerebellum and pons is not well understood.[2]
Outcomes
The severity of different forms of PCH varies, but many children inheriting the mutated gene responsible do not survive infancy or childhood; nevertheless, some individuals born with PCH have reached adulthood.[2]
See also
References
- ↑ Millen KJ, Gleeson JG (February 2008). "Cerebellar development and disease". Curr Opin Neurobiol. 18 (1): 12–9. doi:10.1016/j.conb.2008.05.010. PMC 2474776. PMID 18513948.
- ↑ 2.0 2.1 2.2 2.3 2.4 2.5
- ↑ Online Mendelian Inheritance in Man (OMIM) 607596
- ↑ Online Mendelian Inheritance in Man (OMIM) 608027
- ↑
- ↑
- ↑ Online Mendelian Inheritance in Man (OMIM) 615809
- ↑