Polr3-Related Leukodystrophy

Clinical characteristics.

POLR3-related leukodystrophy, a hypomyelinating leukodystrophy with specific features on brain MRI, is characterized by varying combinations of four major clinical findings:

• Neurologic dysfunction, typically predominated by motor dysfunction (progressive cerebellar dysfunction, and to a lesser extent extrapyramidal [i.e., dystonia], pyramidal [i.e., spasticity] and cognitive dysfunctions)
• Abnormal dentition (delayed dentition, hypodontia, oligodontia, and abnormally placed or shaped teeth)
• Endocrine abnormalities such as short stature (in ~50% of individuals) with or without growth hormone deficiency, and more commonly, hypogonadotropic hypogonadism manifesting as delayed, arrested, or absent puberty
• Ocular abnormality in the form of myopia, typically progressing over several years and becoming severe

POLR3-related leukodystrophy and 4H leukodystrophy are the two recognized terms for five previously described overlapping clinical phenotypes (initially described as distinct entities before their molecular basis was known). These include:

• Hypomyelination, hypodontia, hypogonadotropic hypogonadism (4H syndrome);
• Ataxia, delayed dentition, and hypomyelination (ADDH);
• Tremor-ataxia with central hypomyelination (TACH);
• Leukodystrophy with oligodontia (LO);
• Hypomyelination with cerebellar atrophy and hypoplasia of the corpus callosum (HCAHC).

Age of onset is typically in early childhood but later-onset cases have also been reported.

An infant with Wiedemann-Rautenstrauch syndrome (neonatal progeroid syndrome) was recently reported to have pathogenic variants in POLR3A on exome sequencing. Confirmation of this as a very severe form of POLR3-related leukodystrophy awaits replication in other individuals with a clinical diagnosis of Wiedemann-Rautenstrauch syndrome.

Diagnosis/testing.

POLR3-related leukodystrophy is diagnosed by the combination of classic clinical findings, typical brain MRI features, and the presence of biallelic pathogenic variants in POLR3A, POLR3B, or POLR1C.

Management.

Treatment of manifestations: Individualized care by a multidisciplinary team including a pediatric neurologist, clinical geneticist, physiotherapist, occupational therapist, speech and language pathologist, neuropsychologist, rehabilitation physician, dentist, endocrinologist, ophthalmologist, ear-nose-and-throat specialist, and primary care physician is recommended. Special caution needs to be taken when managing dysphagia in this disorder as it is known to vary widely, even in a single day. Swallowing difficulties will progress over time and dystonia should be monitored and treated to prevent complications and improve the quality of life.

Genetic counseling.

POLR3-related leukodystrophy is inherited in an autosomal recessive manner. At conception, each sib of an affected individual has a 25% chance of being affected, a 50% chance of being an asymptomatic carrier, and a 25% chance of being unaffected and not a carrier. Carrier testing for at-risk relatives and prenatal diagnosis for pregnancies at increased risk are possible if both pathogenic variants in the family are known.

Suggestive Findings

POLR3-related leukodystrophy should be suspected in individuals with the following major/shared clinical features, which may or may not be present:

• Neurologic dysfunction: progressive cerebellar features, including:
  • Gait ataxia, dysarthria, dysmetria, tremor, eye movement abnormalities; and
  • To a lesser extent, extrapyramidal (typically dystonia), pyramidal, and cognitive features
• Abnormal dentition (e.g., hypodontia, oligodontia, delayed teeth eruption) [Wolff et al 2010]
• Endocrine abnormalities such as short stature (in ~50% of individuals) with or without growth hormone deficiency, and more commonly, hypogonadotropic hypogonadism manifesting as delayed, arrested, or absent puberty
• Ocular abnormality in the form of myopia, typically progressing over several years and becoming severe

Note: Although this tetrad is highly suggestive of the diagnosis, not all features are present in all individuals who have POLR3-related leukodystrophy.

Brain MRI findings

• A hypomyelinating leukodystrophy pattern characterized by T₂ mild hyperintensity of the white matter and T₁ hyperintensity, isointensity, or mild hypointensity of the white matter when compared with grey matter structures [Schiffmann & van der Knaap 2009]
• Relative preservation of myelination of specific brain structures, i.e. T₂ hypointense signal (normal or almost normal white matter signal) of the dentate nuclei, anterolateral nuclei of the thalami, globi pallidi, pyramidal tracts in the posterior limbs of the internal capsules, and optic radiations [Steenweg et al 2010, La Piana et al 2014, Wolf et al 2014]
• Variably present: cerebellar atrophy and thinning of the corpus callosum [La Piana et al 2014, Wolf et al 2014]
• Rarely, an atypical MRI pattern with either
  • Selective hypomyelination of the corticospinal tracts; or
  • Cerebellar atrophy with or without focal hypomyelination [La Piana et al 2016]; or
  • Involvement of the striata and red nuclei [Azmanov et al 2016]

See Figure 1.

Figure 1.

MRI of the brain of an individual with molecularly confirmed 4H syndrome A. Sagittal T₁-weighted image (midline) showing cerebellar atrophy (arrowhead) as well as a thin corpus callosum (arrow).

Establishing the Diagnosis

The diagnosis of POLR3-related leukodystrophy is established in a proband with the combination of classic clinical findings, typical brain MRI features, and the identification of biallelic pathogenic variants in POLR3A, POLR3B, or POLR1C on molecular genetic testing (see Table 1).

Molecular testing approaches can include serial single-gene testing, use of a multigene panel, and more comprehensive genomic testing.

Serial single-gene testing. The order of genes to be tested depends on ancestry of the individual:

• In French-Canadian individuals, sequencing of POLR3A should be performed first and followed by gene-targeted deletion/duplication analysis if only one or no pathogenic variant is found.
  • If no pathogenic variant is found, sequencing of POLR3B is performed, followed by gene-targeted deletion/duplication analysis if only one or no pathogenic variant is found.
• For individuals of European ancestry sequencing of POLR3B should be performed first.
  • If a single variant is detected, gene-targeted deletion/duplication analysis of POLR3B is done.
  • If no pathogenic variant is found, sequencing of POLR3A is performed, followed by gene-targeted deletion/duplication analysis if only one or no pathogenic variant is found.
• For individuals from the non-French-Canadian and non-European ancestry, sequencing can start with either POLR3A or POLR3B, followed by gene-targeted deletion/duplication analysis if only one or no pathogenic variant is found.

POLR1C is tested when sequencing and deletion/duplication analysis of POLR3A and POLR3B are both negative.

A multigene panel that includes POLR3A, POLR3B, POLR1C with or without other genes of interest (see Differential Diagnosis) may also be considered. Note: (1) The genes included and the sensitivity of multigene panels vary by laboratory and are likely to change over time. (2) Some multigene panels may include genes not associated with the condition discussed in this GeneReview; thus, clinicians need to determine which multigene panel provides the best opportunity to identify the genetic cause of the condition at the most reasonable cost while limiting identification of pathogenic variants in genes that do not explain the underlying phenotype. (3) Methods used in a panel may include sequence analysis, deletion/duplication analysis, and/or other non-sequencing-based tests.

For an introduction to multigene panels click here. More detailed information for clinicians ordering genetic tests can be found here.

More comprehensive genomic testing (when available) including exome sequencing and genome sequencing may be considered. Such testing may provide or suggest a diagnosis not previously considered (e.g., mutation of a different gene or genes that results in a similar clinical presentation). For an introduction to comprehensive genomic testing click here. More detailed information for clinicians ordering genomic testing can be found here.

Clinical Description

POLR3-related leukodystrophy is a hypomyelinating leukodystrophy characterized by neurologic (cerebellar, extrapyramidal, pyramidal, and cognitive) and non-neurologic (dental, endocrine, and ocular) features.

Before the identification of the involved genes, five overlapping clinical phenotypes were described and are now all recognized as part of the spectrum of POLR3-related leukodystrophy:

• 4H syndrome. Hypomyelination, hypodontia, hypogonadotropic hypogonadism [Wolf et al 2005, Timmons et al 2006, Vázquez-López et al 2008]
• ADDH. Ataxia, delayed dentition, and hypomyelination [Wolf et al 2007, Wolff et al 2010]
• TACH. Tremor-ataxia with central hypomyelination [Bernard et al 2010, Bernard et al 2011, Tétreault et al 2011, Tétreault et al 2012]
• LO. Leukodystrophy with oligodontia [Atrouni et al 2003, Chouery et al 2011]
• HCAHC. Hypomyelination with cerebellar atrophy and hypoplasia of the corpus callosum [Sasaki et al 2009, Saitsu et al 2011]

Age of onset is typically in early childhood but later-onset cases have also been reported.

Neurologic dysfunction includes prominent cerebellar features leading to progressive gait abnormalities, dysmetria, dysdiadochokinesis, dysarthria, and extraocular movement abnormalities including progressive loss of pursuits (saccadic ocular pursuits), abnormal saccades (i.e., hypo- or hypermetric), and gaze-evoked nystagmus. Progressive vertical more than horizontal gaze restriction has also been reported. Hypersalivation and dysphagia are also commonly seen, typically later in the disease course.

• Individuals may also develop extrapyramidal features – almost always dystonia.
• Mild pyramidal features are typically present but are not problematic in the vast majority of individuals.
• An upper-extremity tremor (usually cerebellar in nature) with or without a dystonic component may be a presenting sign.
• Cognitive decline typically occurs later, except in late-onset cases.
• Approximately 10% of individuals have later onset and slower progression; they typically present with academic difficulties and cognitive decline which manifests as a plateau in learning at school. Those with later onset may have also behavioral abnormalities.

Dental abnormalities include delayed dentition, hypodontia, oligodontia, and eruption of abnormally placed or shaped teeth, among others [Wolff et al 2010]. Dental abnormalities may be subtle and have not been seen in all individuals.

Endocrine abnormalities. Hypogonadotropic hypogonadism (HH), the most typical endocrine characteristic, is note seen in all individuals. When reported, HH typically presents with delayed or arrested puberty or absence of early pubertal changes. Other reported endocrine abnormalities include short stature (in 50% of individuals [Wolf et al 2014]) and growth hormone deficiency [Potic et al 2012, Billington et al 2015, Potic et al 2015].

Ocular abnormality. Myopia, typically progressive over several years and eventually leading to severe myopia, is the most common non-neurologic feature.

Course and life span. The course of POLR3-related leukodystrophy is invariably progressive. Life span depends on the supportive measures put in place to prevent secondary complications. POLR3-related leukodystrophy is considered to be a life-limiting condition; those with earlier onset are at a higher risk for mortality in young adulthood. Individuals with later onset or with a slower progressive disease course could survive later into adulthood (i.e., 4^th-5^th decade).

Additional features seen less frequently include the following [Wolf et al 2005, Timmons et al 2006, Vázquez-López et al 2008, Bekiesinska-Figatowska et al 2010, Orcesi et al 2010, Wolff et al 2010, Sato et al 2011, Potic et al 2012]:

• Neurologic. Seizures reported in a minority of individuals [Bernard et al 2011, Wolf et al 2014]
• Ocular
  • Optic atrophy
  • Cataracts reported in four individuals [Sato et al 2011, Wolf et al 2014]

Neurophysiologic investigations. All affected individuals undergoing EMG and nerve conduction studies had normal results [Author, personal observation].

Wiedemann-Rautenstrauch syndrome (neonatal progeroid syndrome). A newborn with features of this disorder (including extreme small size, sparse scalp hair, broad abnormally shaped skull, triangular face with midface retraction, natal teeth, decreased subcutaneous fat, and limb contractures) was recently reported to have biallelic truncating variants in POLR3A on exome sequencing that were predicted to result in little residual POLR3 function. Confirmation of this as a very severe form of POLR3-related leukodystrophy awaits replication in other patients with a clinical diagnosis of Wiedemann-Rautenstrauch syndrome [Jay et al 2016].

Genotype-Phenotype Correlations

POLR3A

• Individuals with POLR3A pathogenic variants tend to have a later disease onset than those with POLR3B pathogenic variants but more rapid disease progression [Wolf et al 2014].
• A single female infant with Wiedemann-Rautenstrauch syndrome (neonatal progeroid syndrome) was recently reported to have biallelic truncating pathogenic variants in POLR3A [Jay et al 2016].

POLR3B

• Individuals with POLR3B pathogenic variants have earlier disease onset than those with POLR3A pathogenic variants but a slower disease course.
• Those with POLR3B pathogenic variants are more likely to have cerebellar atrophy on MRI and preservation of the myelination of the corticospinal tracts at the level of the internal capsules, compared to individuals with POLR3A pathogenic variants.
• The common POLR3B pathogenic variant c.1568T>A (p.Val523Glu) is very mild. Indeed, individuals homozygous for this variant were either asymptomatic or very mildly symptomatic in early adulthood [Wolf et al 2014].

POLR1C. Limited information is available on individuals with POLR1C pathogenic variants.

Prevalence

The prevalence of POLR3-related leukodystrophy is unknown.

Individuals with POLR3-related leukodystrophy have been identified worldwide [Atrouni et al 2003, Sasaki et al 2009, Bekiesinska-Figatowska et al 2010, Saitsu et al 2011, Sato et al 2011, Wolf et al 2014].

Evaluations Following Initial Diagnosis

To establish the extent of disease and needs of an individual diagnosed with a POLR3-related leukodystrophy, the following are recommended:

• Pediatric neurology consultation
• Swallowing assessment
• Physiotherapy evaluation
• Occupational therapy evaluation
• Speech and language pathology assessment
• Rehabilitation physician (i.e., physiatrist) consultation
• Neuropsychology evaluation
• Brain MRI, if not performed at the time of diagnosis
• Dentistry consultation
• Endocrine consultation
• Ophthalmologic evaluation
• Ear-nose-and-throat specialist consultation for hypersalivation and swallowing issues
• Consultation with a clinical geneticist and/or genetic counselor

Treatment of Manifestations

Individualized care by a multidisciplinary team including a pediatric neurologist, clinical geneticist, physiotherapist, occupational therapist, speech and language pathologist, neuropsychologist, rehabilitation physician, dentist, endocrinologist, ophthalmologist, ear-nose-and-throat specialist, and primary care physician is recommended.

Manifestations such as ambulation difficulties and seizures are managed in a routine manner.

Special caution needs to be taken when managing dysphagia in this disorder as it is known to be quite variable, even in a single day. This is probably due to the prominent cerebellar involvement, leading to more incoordination of swallowing with fatigue, but also with some unpredictability. Dysphagia management is therefore important. Swallowing difficulties will progress over time and individuals may require gastrostomy to manage nutrition.

Spasticity and dystonia should be monitored and treated to prevent complications and to improve the quality of life.

Hypersalivation is managed with the multidisciplinary team and an otolaryngologist. Treatment must be individualized. Therapies to consider include rehabilitation (e.g., oromotor therapy, behavioral therapy); medical therapy (e.g., anticholinergic medications, botulinum toxin injections); and, in severe cases, surgery (e.g., relocation of the parotid ducts and relocation of the submandibular ducts with or without sublingual gland excision).

Learning difficulties are likely to progress slowly. The cognitive involvement is typically much less severe than the motor involvement. In contrast, activities of daily living are likely to become problematic early on in the disease course as motor difficulties make patients progressively more dependent on assistance from others.

Dental manifestations should be managed, when necessary, by a dentist and/or orthodontist.

Patients should be followed regularly by an endocrinologist. The decision to treat sex and growth hormone deficiency, when present, should be made on an individual basis.

Patients need to be followed regularly by an ophthalmologist. A significant proportion of patients will have progressive myopia over several years, which will become severe before stabilizing.

Surveillance

No general surveillance guidelines have been developed to date; monitoring should be individualized.

Agents/Circumstances to Avoid

Avoid the following:

• Foods that are likely to lead to choking
• Medications acting on D2 receptor blockers (e.g., neuroleptics such as haloperidol or risperidone, anti-nausea medications such as metoclopramide) as these can exacerbate the extrapyramidal features

Evaluation of Relatives at Risk

See Genetic Counseling for issues related to testing of at-risk relatives for genetic counseling purposes.

Therapies Under Investigation

Search ClinicalTrials.gov and EU Clinical Trials Register in Europe for access to information on clinical studies for a wide range of diseases and conditions. Note: There may not be clinical trials for this disorder.