U.S. flag

An official website of the United States government

Format

Send to:

Choose Destination

Morquio syndrome

MedGen UID:
44513
Concept ID:
C0026707
Disease or Syndrome
Synonyms: Eccentrochondrodysplasia; MPS IV; Mucopolysaccharidosis type 4; Mucopolysaccharidosis, Type IV
SNOMED CT: Morquio syndrome (378007); Chondro-osteodystrophy (378007); Morquio-Suarez syndrome (378007); Morquio-Ullrich disease (378007); Osteochondrodystrophia deformans (378007); Atypical chondrodystrophy (378007); Morquio disease (378007); Familial osteochondrodystrophy (378007); Brailsford-Morquio syndrome (378007); Hereditary enchondral dysostosis (378007); Chondrodystrophia tarda (378007); Familial osseous dystrophy (378007); Keratan sulfaturia (378007); Mucopolysaccharidosis, MPS-IV (378007); Morquio-Brailsford disease (378007); Osteochondrodystrophy (378007); Mucopolysaccharidosis type IV (378007)
Modes of inheritance:
Autosomal recessive inheritance
MedGen UID:
141025
Concept ID:
C0441748
Intellectual Product
Source: Orphanet
A mode of inheritance that is observed for traits related to a gene encoded on one of the autosomes (i.e., the human chromosomes 1-22) in which a trait manifests in individuals with two pathogenic alleles, either homozygotes (two copies of the same mutant allele) or compound heterozygotes (whereby each copy of a gene has a distinct mutant allele).
 
Related genes: GLB1, GALNS
 
Monarch Initiative: MONDO:0018938
Orphanet: ORPHA582

Definition

The life expectancy of individuals with MPS IV depends on the severity of symptoms. Severely affected individuals may survive only until late childhood or adolescence. Those with milder forms of the disorder usually live into adulthood, although their life expectancy may be reduced. Spinal cord compression and airway obstruction are major causes of death in people with MPS IV.

Mucopolysaccharidosis type IV (MPS IV), also known as Morquio syndrome, is a progressive condition that mainly affects the skeleton. The rate at which symptoms worsen varies among affected individuals.

The first signs and symptoms of MPS IV usually become apparent during early childhood. Affected individuals develop various skeletal abnormalities, including short stature, knock knees, and abnormalities of the ribs, chest, spine, hips, and wrists. People with MPS IV often have joints that are loose and very flexible (hypermobile), but they may also have restricted movement in certain joints. A characteristic feature of this condition is underdevelopment (hypoplasia) of a peg-like bone in the neck called the odontoid process. The odontoid process helps stabilize the spinal bones in the neck (cervical vertebrae). Odontoid hypoplasia can lead to misalignment of the cervical vertebrae, which may compress and damage the spinal cord, resulting in paralysis or death.

In people with MPS IV, the clear covering of the eye (cornea) typically becomes cloudy, which can cause vision loss. Some affected individuals have recurrent ear infections and hearing loss. The airway may become narrow in some people with MPS IV, leading to frequent upper respiratory infections and short pauses in breathing during sleep (sleep apnea). Other common features of this condition include mildly "coarse" facial features, thin tooth enamel, multiple cavities, heart valve abnormalities, a mildly enlarged liver (hepatomegaly), and a soft out-pouching around the belly-button (umbilical hernia) or lower abdomen (inguinal hernia). Unlike some other types of mucopolysaccharidosis, MPS IV does not affect intelligence. [from MedlinePlus Genetics]

Professional guidelines

PubMed

Sawamoto K, Álvarez González JV, Piechnik M, Otero FJ, Couce ML, Suzuki Y, Tomatsu S
Int J Mol Sci 2020 Feb 23;21(4) doi: 10.3390/ijms21041517. PMID: 32102177Free PMC Article
Chien YH, Lee NC, Chen PW, Yeh HY, Gelb MH, Chiu PC, Chu SY, Lee CH, Lee AR, Hwu WL
Orphanet J Rare Dis 2020 Feb 3;15(1):38. doi: 10.1186/s13023-020-1322-z. PMID: 32014045Free PMC Article
Hendriksz CJ, Al-Jawad M, Berger KI, Hawley SM, Lawrence R, Mc Ardle C, Summers CG, Wright E, Braunlin E
J Inherit Metab Dis 2013 Mar;36(2):309-22. Epub 2012 Feb 23 doi: 10.1007/s10545-012-9459-0. PMID: 22358740Free PMC Article

Recent clinical studies

Etiology

Sahin MC, Ipek EM, Zinnuroglu M, Borcek AO
Childs Nerv Syst 2023 May;39(5):1323-1328. Epub 2022 Nov 18 doi: 10.1007/s00381-022-05748-5. PMID: 36400977
Yahanda AT, Chicoine MR
World Neurosurg 2020 Jul;139:151-157. Epub 2020 Apr 17 doi: 10.1016/j.wneu.2020.04.016. PMID: 32305599
Charrow J, Alden TD, Breathnach CA, Frawley GP, Hendriksz CJ, Link B, Mackenzie WG, Manara R, Offiah AC, Solano ML, Theroux M
Mol Genet Metab 2015 Jan;114(1):11-8. Epub 2014 Oct 30 doi: 10.1016/j.ymgme.2014.10.010. PMID: 25496828
McKay SD, Al-Omari A, Tomlinson LA, Dormans JP
Spine (Phila Pa 1976) 2012 Mar 1;37(5):E269-77. doi: 10.1097/BRS.0b013e31823b3ded. PMID: 22045003
Parkinson-Lawrence EJ, Muller VJ, Hopwood JJ, Brooks DA
Clin Chim Acta 2007 Feb;377(1-2):88-91. Epub 2006 Sep 1 doi: 10.1016/j.cca.2006.08.030. PMID: 17027703

Diagnosis

Aubeleau M, David T, Gascon P
Ophthalmol Retina 2024 Oct;8(10):e30. Epub 2024 Mar 23 doi: 10.1016/j.oret.2024.02.014. PMID: 38520463
Campbell JW
Neurosurg Clin N Am 2022 Jan;33(1S):e1-e10. Epub 2022 Aug 6 doi: 10.1016/j.nec.2022.02.001. PMID: 36115686
Sawamoto K, Álvarez González JV, Piechnik M, Otero FJ, Couce ML, Suzuki Y, Tomatsu S
Int J Mol Sci 2020 Feb 23;21(4) doi: 10.3390/ijms21041517. PMID: 32102177Free PMC Article
Chien YH, Lee NC, Chen PW, Yeh HY, Gelb MH, Chiu PC, Chu SY, Lee CH, Lee AR, Hwu WL
Orphanet J Rare Dis 2020 Feb 3;15(1):38. doi: 10.1186/s13023-020-1322-z. PMID: 32014045Free PMC Article
Holzgreve W, Gröbe H, von Figura K, Kresse H, Beck H, Mattei JF
Hum Genet 1981;57(4):360-5. doi: 10.1007/BF00281685. PMID: 6793501

Therapy

Yahanda AT, Chicoine MR
World Neurosurg 2020 Jul;139:151-157. Epub 2020 Apr 17 doi: 10.1016/j.wneu.2020.04.016. PMID: 32305599
Valayannopoulos V, Wijburg FA
Rheumatology (Oxford) 2011 Dec;50 Suppl 5:v49-59. doi: 10.1093/rheumatology/ker396. PMID: 22210671
Mettananda DS, Fernando AD
Ceylon Med J 2008 Mar;53(1):24-5. doi: 10.4038/cmj.v53i1.223. PMID: 18590267
Huang KC, Sukegawa K, Orii T
Clin Chim Acta 1985 Sep 30;151(2):141-6. doi: 10.1016/0009-8981(85)90317-1. PMID: 3930102
Beighton P, Craig J
J Bone Joint Surg Br 1973 Aug;55(3):478-81. PMID: 4269648

Prognosis

Averill LW, Kecskemethy HH, Theroux MC, Mackenzie WG, Pizarro C, Bober MB, Ditro CP, Tomatsu S
Pediatr Radiol 2021 Jun;51(7):1202-1213. Epub 2021 Feb 20 doi: 10.1007/s00247-020-04946-0. PMID: 33608742Free PMC Article
Chien YH, Lee NC, Chen PW, Yeh HY, Gelb MH, Chiu PC, Chu SY, Lee CH, Lee AR, Hwu WL
Orphanet J Rare Dis 2020 Feb 3;15(1):38. doi: 10.1186/s13023-020-1322-z. PMID: 32014045Free PMC Article
Kaissi AA, van Egmond-Fröhlich A, Ryabykh S, Ochirov P, Kenis V, Hofstaetter JG, Grill F, Ganger R, Kircher SG
Medicine (Baltimore) 2016 Dec;95(50):e5505. doi: 10.1097/MD.0000000000005505. PMID: 27977582Free PMC Article
Nelson J, Crowhurst J, Carey B, Greed L
Am J Med Genet A 2003 Dec 15;123A(3):310-3. doi: 10.1002/ajmg.a.20314. PMID: 14608657
Barker D, Welbury RR
ASDC J Dent Child 2000 Nov-Dec;67(6):431-3, 407. PMID: 11204070

Clinical prediction guides

Chien YH, Lee NC, Chen PW, Yeh HY, Gelb MH, Chiu PC, Chu SY, Lee CH, Lee AR, Hwu WL
Orphanet J Rare Dis 2020 Feb 3;15(1):38. doi: 10.1186/s13023-020-1322-z. PMID: 32014045Free PMC Article
Hughes D, Giugliani R, Guffon N, Jones SA, Mengel KE, Parini R, Matousek R, Hawley SM, Quartel A
Orphanet J Rare Dis 2017 May 23;12(1):98. doi: 10.1186/s13023-017-0634-0. PMID: 28535791Free PMC Article
Khan MA, Addison O, James A, Hendriksz CJ, Al-Jawad M
Micron 2016 Apr;83:48-53. Epub 2016 Jan 12 doi: 10.1016/j.micron.2016.01.001. PMID: 26896739
Davison JE, Kearney S, Horton J, Foster K, Peet AC, Hendriksz CJ
J Inherit Metab Dis 2013 Mar;36(2):323-8. Epub 2012 Jan 10 doi: 10.1007/s10545-011-9430-5. PMID: 22231379
Atinga M, Hamer AJ
J Bone Joint Surg Br 2008 Dec;90(12):1631-3. doi: 10.1302/0301-620X.90B12.20641. PMID: 19043137

Recent systematic reviews

Yahanda AT, Chicoine MR
World Neurosurg 2020 Jul;139:151-157. Epub 2020 Apr 17 doi: 10.1016/j.wneu.2020.04.016. PMID: 32305599

Supplemental Content

Table of contents

    Clinical resources

    Practice guidelines

    • PubMed
      See practice and clinical guidelines in PubMed. The search results may include broader topics and may not capture all published guidelines. See the FAQ for details.

    Recent activity

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

    See more...