Bruck syndrome

Bruck syndrome is characterized as the combination of arthrogryposis multiplex congenita and osteogenesis imperfecta. Both diseases are uncommon, but concurrence is extremely rare which makes Bruck syndrome very difficult to research.[1] Bruck syndrome is thought to be an atypical variant of osteogenesis imperfecta most resembling type III, if not its own disease.[2][3] Multiple gene mutations associated with osteogenesis imperfecta are not seen in Bruck syndrome. Many affected individuals are within the same family, and pedigree data supports that the disease is acquired through autosomal recessive inheritance.[4] Bruck syndrome has features of congenital contractures, bone fragility, recurring bone fractures, flexion joint and limb deformities, pterygia, short body height, and progressive kyphoscoliosis. Individuals encounter restricted mobility and pulmonary function. A reduction in bone mineral content and larger hydroxyapatite crystals are also detectable[5] Joint contractures are primarily bilateral and symmetrical, and most prone to ankles.[3] Bruck syndrome has no effect on intelligence, vision, or hearing.[4]


The first case was in 1897 of a male who was described by Bruck as having bone fragility and bone contractures.[4] Bruck was credited with the first description and the disease’s eponym.[1]


Diagnosis of Bruck syndrome must distinguish the association of contractures and skeletal fragility. Ultrasound is used for prenatal diagnosis. The diagnosis of a neonate bears resemblance to arthrogryposis multiplex congenital, and later in childhood to osteogenesis imperfecta.[1]


Until more molecular and clinical studies are performed there will be no way to prevent the disease. Treatments are directed towards alleviating the symptoms. To treat the disease it is crucial to diagnose it properly.[6] Orthopedic therapy and fracture management are necessary to reduce the severity of symptoms. Bisphosphonate drugs are also an effective treatment.[4]

Genetics and Mechanism

The genetics of Bruck syndrome differs from osteogenesis imperfecta. Osteogenesis imperfecta involves autosomal dominant mutations to Col 1A2 or Col 1A2 which encode type 1 procollagen.[6] Bruck syndrome is linked to mutations in two genes, and therefore is divided in two types. Bruck syndrome type 1 is caused by a homozygous mutation in the FKBP10 gene. It encodes FKBP65, an endoplasmic reticulum associated peptidyl-prolyl cis/trans isomerase (PPIase) that functions as a chaperone in collagen biosynthesis. Osteoblasts deficient in FKBP65 have a buildup of procollagen aggregates in the endoplasmic reticulum which reduces their ability to form bone.[7] Furthermore, Bruck syndrome type 1 patients have under-hydroxylated lysine residues in the collagen telopeptide and as a result show diminished hydroxylysylpyridinoline cross-links. Type 2 is caused by a homozygous mutation in the PLOD2 gene. It encodes the enzyme, lysyl hydroxylase 2, which catalyzes hydroxylation of lysine residues in collagen cross-links. PLOD2 is most expressed in active osteoblasts since collagen cross-linking is tissue-specific. Mutation in PLOD2 alters the structure of telopeptide lysyl hydroxylase and prevents fibril formation of collagen type 1. Bone analysis shows the lysine residues of telopeptides in collagen type 1 are under-hydroxylated.[6]


  1. 1 2 3 Mokete, L.; Robertson, A.; Viljoen, D.; Beighton, Peter (2005). "Bruck syndrome: congenital joint contractures with bone fragility". Journal of Orthopaedic Science. 10 (6): 641–646. doi:10.1007/s00776-005-0958-9. PMID 16307191.
  2. Berg, C.; Geipel, A.; Noack et. al, F (2005). "Mutations in FKBP10 cause recessive osteogenesis imperfecta and bruck syndrome". Prenatal Diagnosis. 25 (3): 545–548. doi:10.1002/jbmr.250.
  3. 1 2 Blacksin, M.; Pletcher, B.; David et. al, Miriam (1998). "Osteogenesis imperfecta with joint contractures: Bruck syndrome". Pediatric Radiology. 28(2) (2): 117–119. doi:10.1007/s002470050309.
  4. 1 2 3 4 Datta, V.; Sinha, A.; Saili et. al, A. (2005). "Osteogenesis Imperfecta". Journal of Pediatrics. 72(5) (5): 441–442. doi:10.1007/BF02731745.
  5. Banks, R.; Robins, S.; Wijmenga et. al, . (1999). "Defective collagen crosslinking in bone, but not in ligament or cartilage, in Bruck syndrome: Indications for a bone-specific telopeptide lysyl hydroxylase on chromosome 17". Proceedings of the National Academy of Sciences. 96 (3): 1054–1058. PMC 15349Freely accessible.
  6. 1 2 3 Yapicioglu, H.; Ozcan, K.; Arikan et. al, O. (2009). "Bruck syndrome: osteogenesis imperfecta and arthrogryposis multiplex congenital". Annals of Tropical Paediactrics. 29: 159–1662.
  7. Shaheen, Ranad; Al-Owain, Mohammed; Faqeih, Eissa; Al-Hashmi, Nadia; Awaji, Ali; Al-Zayed, Zayed; Alkuraya, Fowzan S (2011). "Mutations in FKBP10 cause both Bruck syndrome and isolated osteogenesis imperfecta in humans". American Journal of Medical Genetics Part A. 155 (6): 1448–1452. doi:10.1002/ajmg.a.34025.

Further reading

This article is issued from Wikipedia - version of the 10/3/2016. The text is available under the Creative Commons Attribution/Share Alike but additional terms may apply for the media files.