Behr syndrome
Behr syndrome | |
---|---|
Classification and external resources | |
ICD-10 | G11.18 |
OMIM | 210000 |
DiseasesDB | 32611 |
MeSH | C537669 |
Behr syndrome is characterized by the association of early-onset optic atrophy with spinocerebellar degeneration resulting in ataxia, pyramidal signs, peripheral neuropathy and developmental delay.[1][2]
Although it is an autosomal recessive disorder, heterozygotes may still manifest much attenuated symptoms.[3] Autosomal dominant inheritance also being reported in a family.[4] Recently a variant of OPA1 mutation with phenotypic presentation like Behr syndrome is also described.[5] Some reported cases have been found to carry mutations in the OPA1, OPA3 or C12ORF65 genes which are known causes of pure optic atrophy or optic atrophy complicated by movement disorder.[6]
Clinical Features
Onset : Early childhood
Progression: Chronic progressive
Clinical: Cerebellar ataxia plus syndrome / Optic Atrophy Plus Syndrome
Neurological:
Ocular: Optic atrophy, nystagmus, scotoma, and bilateral retrobulbar neuritis.
Other: Mental retardation, myoclonic epilepsy, spasticity, and posterior column sensory loss. Tremor in some cases.[7]
Musculoskeletal
Contractures, lower limbs , Achilles tendon contractures , Hamstring contractures , Adductor longus contractures[8]
Systemic
Hypogonadotrophic hypogonadism.[9]
Neuroimaging
MRI
Diffuse, symmetric white matter abnormalities were demonstrated by magnetic resonance imaging suggesting that Behr syndrome may represent a disorder of white matter associated with an unknown biochemical abnormality.[10]
Genetics
![](../I/m/Autorecessive.svg.png)
Behr syndrome is autosomal recessive which means the defective gene is located on an autosome, and two copies of the gene - one inherited from each parent - are required to be born with the disorder. The parents of an individual with an autosomal recessive disorder both carry one copy of the defective gene, but are usually not affected by the disorder. Autosomal dominant inheritance also being reported.[4]
Compound heterozygous mutations in OPA1 gene were reported.[5][11] Molecular genetic studies revealed a homozygous mutation in the C19ORF12 gene which has been previously reported in patients with a subtype of NBIA (neurodegeneration with brain iron accumulation), mitochondrial membrane protein-associated neurodegeneration (MPAN).[6]
Pathology
Autopsy on one of the sister with Behr Syndrome revealed central atrophy of the optic nerves and total disarray of the normal laminar pattern of the lateral geniculate nucleus, dropout of neurons, and gliosis. There were numerous axonal spheroids in the neuropil. Similar spheroids with cell loss and gliosis were also observed in other thalamic nuclei and, rarely, in the pallida.[12]
Diagnosis
Diagnosis is suspected clinically and family history, neuroimaging and genetic study helps to confirm Behr Syndrome.
Treatment
Supportive
See also
- List of systemic diseases with ocular manifestations
- Leber's Hereditary Optic Atrophy
- Mitochondrial Disorders
- Optic Atrophy
References
- ↑ synd/3048 at Who Named It?
- ↑ Behr C (1909). "Die komplizierte, hereditär-familiäre Optikusatrophie des Kindesalters: ein bisher nicht beschriebener Symptomkompleks.". Klinische Monatsblätter für Augenheilkunde. 47: 138–60.
- ↑ Van Bogaert, L (1942). "Premiere observation anatomo-clinique de l'atrophie optique heredofamiliale compliquee de Behr". Bull. Acad. Roy. Med. Belg.
- 1 2 Felicio, Andre C.; Godeiro-Junior, Clecio; Alberto, Lucianna G.; Pinto, Aline P. M.; Sallum, Juliana M. F.; Teive, Helio G.; Barsottini, Orlando G. P. (2008-01-01). "Familial Behr syndrome-like phenotype with autosomal dominant inheritance". Parkinsonism & Related Disorders. 14 (4): 370–372. doi:10.1016/j.parkreldis.2007.08.008. ISSN 1353-8020. PMID 17977780.
- 1 2 Marelli, Cecilia; Amati-Bonneau, Patrizia; Reynier, Pascal; Layet, Valérie; Layet, Antoine; Stevanin, Giovanni; Brissaud, Etienne; Bonneau, Dominique; Durr, Alexandra (2011-04-01). "Heterozygous OPA1 mutations in Behr syndrome". Brain: A Journal of Neurology. 134 (Pt 4): e169; author reply e170. doi:10.1093/brain/awq306. ISSN 1460-2156. PMID 21112924.
- 1 2 Kleffner, Ilka; Wessling, Caroline; Gess, Burkhard; Korsukewitz, Catharina; Allkemper, Thomas; Schirmacher, Anja; Young, Peter; Senderek, Jan; Husstedt, Ingo W. (2015-10-15). "Behr syndrome with homozygous C19ORF12 mutation". Journal of the Neurological Sciences. 357 (1-2): 115–118. doi:10.1016/j.jns.2015.07.009. ISSN 1878-5883. PMID 26187298.
- ↑ Schramm, P.; Scheihing, M.; Rasche, D.; Tronnier, V. M. (2005-06-01). "Behr syndrome variant with tremor treated by VIM stimulation". Acta Neurochirurgica. 147 (6): 679–683; discussion 683. doi:10.1007/s00701-005-0508-4. ISSN 0001-6268. PMID 15770348.
- ↑ Copeliovitch, L.; Katz, K.; Arbel, N.; Harries, N.; Bar-On, E.; Soudry, M. (2001-08-01). "Musculoskeletal deformities in Behr syndrome". Journal of Pediatric Orthopedics. 21 (4): 512–514. doi:10.1097/01241398-200107000-00018. ISSN 0271-6798. PMID 11433166.
- ↑ Alfaro, José J.; Aparicio, Manuel; Quintana, Alicia; Barrio, Raquel (2002-05-25). "[Behr syndrome and hypergonadotropic hypogonadism]". Medicina Clínica. 118 (19): 759. doi:10.1016/s0025-7753(02)72522-0. ISSN 0025-7753. PMID 12049713.
- ↑ Marzan, KA (1994). "MRI abnormalities in Behr syndrome.". Pediatr Neurol. PMID 8060430.
- ↑ Bonneau, Dominique; Colin, Estelle; Oca, Florine; Ferré, Marc; Chevrollier, Arnaud; Guéguen, Naïg; Desquiret-Dumas, Valérie; N'Guyen, Sylvie; Barth, Magalie (2014-10-01). "Early-onset Behr syndrome due to compound heterozygous mutations in OPA1". Brain: A Journal of Neurology. 137 (Pt 10): e301. doi:10.1093/brain/awu184. ISSN 1460-2156. PMID 25012220.
- ↑ Horoupian, DS (1979). "Behr syndrome: a clinicopathologic report.". Neurology. 1979 Mar;29(3):323-7. PMID 571977.
External links
- Behr syndrome at NIH's Office of Rare Diseases
- Behr Syndrome at Orphanet
- Behr Syndrome at Omim.com
- Behr Syndrome at University of Arizona