Medicine:Pontocerebellar hypoplasia

Short description: Group of neurodegenerative disorders

Pontocerebellar hypoplasia
Other names	Non-syndromic pontocerebellar hypoplasia
Pontocerebellar hypoplasia is inherited in an autosomal recessive manner
Specialty	Neurology
Treatment	Unknown

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). Where known, these disorders are inherited in an autosomal recessive fashion. There is no known cure for PCH.

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.

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  Facial features (dysmorphism) of patients with one form of pontocerebellar hypoplasia due to mutations in the CASK gene. A and B: patient at 1 year (A) and 4 years (B). C: patient, 18 months. D: patient, 13 years. E: patient, 13 years. F: patient, 12 years. Note minor facial dysmorphism: round face, small chin, well-drawn eyebrows in the younger patients; longer face, high and large nasal bridge, long nose, protruding maxilla, in the older patients.

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  Magnetic resonance imaging (MRI) examples of patients with pontocerebellar hypoplasia with CASK mutations. A. Sagittal images showing different degrees of hypoplasia (incomplete formation) of the pons and vermis (parts of the brain). Numbers represent different patients. Figure 9a shows an MRI of a patient at age 4 months and figure 9b shows the same patient at age 11 years. There is no progression of the lesions between successive MRI in patient 9. Note that in all patients, the pons is very small but has a relative sparing of its bulging, mainly in its superior part. Hypoplasia predominates at the lower part of the pons. Vermis hypoplasia is very variable, severe in patient 13, very slight in patient 10-11-12 and also predominates at the inferior part. B. Coronal images showing varying degrees of cerebellar hemispheric (one of two halves of a part of the brain) hypoplasia. Hemispheres are frequently asymmetric. Note that the vermis does not protrude from the hemispheres indicating similar involvement of the vermis and the hemispheres. This pattern is different from that of PCH2 in which the vermis is relatively spared leading to the classic image of a "dragonfly", the protruding vermis being the body of the dragonfly and the hemispheres, the wings.

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.

Causes

Pontocerebellar hypoplasia is caused by mutations in genes including Sepsecs gene, VRK1 (PCH1); TSEN2, TSEN34 (PCH2); RARS2 (PCH6); and TSEN54 (PCH2 and PCH4). The genes associated with PCH3 and PCH5 have not yet been identified.

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.

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.

Diagnosis

Classification

Pontocerebellar hypoplasia is classified as follows:

Type	OMIM	Gene	Locus	Distinctive features	Alternate names
PCH1A	Online Mendelian Inheritance in Man (OMIM) 607596	VRK1	14q32	Infantile onset anterior horn cell degeneration resulting in progressive muscle atrophy; resembles infantile spinal muscular atrophy	Spinal muscular atrophy with pontocerebellar hypoplasia (SMA-PCH)
PCH1B	Online Mendelian Inheritance in Man (OMIM) 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	Online Mendelian Inheritance in Man (OMIM) 277470	TSEN54	17q25.1	Dyskinetic movements, seizures (frequently)	Volendam neurodegenerative disease
PCH2B	Online Mendelian Inheritance in Man (OMIM) 612389	TSEN2	3p25.2
PCH2C	Online Mendelian Inheritance in Man (OMIM) 612390	TSEN34	19q13.42
PCH2D	Online Mendelian Inheritance in Man (OMIM) 613811	SEPSECS	4p15.2		Progressive cerebello-cerebral atrophy (PCCA)
PCH2E	Online Mendelian Inheritance in Man (OMIM) 615851	VPS53	17p13.3	Profound mental retardation, progressive microcephaly, spasticity, and early-onset epilepsy
PCH2F	Online Mendelian Inheritance in Man (OMIM) 617026	TSEN15	1q25.3	Variable neurologic signs and symptoms, including cognitive and motor delay, poor or absent speech, seizures, and spasticity
PCH3	Online Mendelian Inheritance in Man (OMIM) 608027	PCLO	7q11–q21	Seizures, short stature, optic atrophy, progressive microcephaly, severe developmental delay; described only in a handful of cases.	CLAM-PCH, cerebellar atrophy with progressive microcephaly
PCH4	Online Mendelian Inheritance in Man (OMIM) 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	Online Mendelian Inheritance in Man (OMIM) 610204	TSEN54	17q25.1	Severe prenatal form, described in one family	Olivopontocerebellar hypoplasia (OPCH)
PCH6	Online Mendelian Inheritance in Man (OMIM) 611523	RARS2	6q15	Severe encephalopathy in the newborn with hypotonia, and inconstantly: intractable seizures, edema, increased lactate blood levels, mitochondrial respiratory chain defects
PCH7	Online Mendelian Inheritance in Man (OMIM) 614969	TOE1	1p34.1	Hypotonia, apneic episodes, seizures, vanishing testis
PCH8	Online Mendelian Inheritance in Man (OMIM) 614961	CHMP1A	16q24.3	Severe psychomotor retardation, abnormal movements, hypotonia, spasticity, and variable visual defects
PCH9	Online Mendelian Inheritance in Man (OMIM) 615809	AMPD2	1p13.3	Severely delayed psychomotor development, progressive microcephaly, spasticity, seizures, and brain abnormalities, including brain atrophy, thin corpus callosum, and delayed myelination
PCH10	Online Mendelian Inheritance in Man (OMIM) 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.

Another gene that has been associated with this condition is coenzyme A synthase (COASY).

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.

See also

• Mental retardation and microcephaly with pontine and cerebellar hypoplasia

External links

Classification	D ICD-10: Q04.3
External resources	Orphanet: 98523