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Brachyolmia - Maroteaux type(BCYM2)

MedGen UID:
1777254
Concept ID:
C5399913
Disease or Syndrome
Synonyms: BCYM2; Brachyolmia type 2
SNOMED CT: Brachyolmia - Maroteaux type (389165004)
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).
 
Monarch Initiative: MONDO:0013360
OMIM®: 613678
Orphanet: ORPHA93302

Definition

The term 'brachyolmia' was coined to designate a bone dysplasia characterized clinically by short trunk dwarfism and radiographically by generalized platyspondyly without significant long bone abnormalities. The Maroteaux type of brachyolmia is an autosomal recessive form in which there is rounding of the anterior and posterior vertebral borders, with less elongation on lateral view and less lateral extension on anteroposterior view than is seen in the Hobaek type of brachyolmia (271530). Maroteaux brachyolmia may also be associated with precocious calcification of the falx cerebri, and minor facial anomalies (summary by Shohat et al., 1989). For a discussion of genetic heterogeneity of brachyolmia, see 271530. [from OMIM]

Clinical features

From HPO
Short stature
MedGen UID:
87607
Concept ID:
C0349588
Finding
A height below that which is expected according to age and gender norms. Although there is no universally accepted definition of short stature, many refer to "short stature" as height more than 2 standard deviations below the mean for age and gender (or below the 3rd percentile for age and gender dependent norms).
Platyspondyly
MedGen UID:
335010
Concept ID:
C1844704
Finding
A flattened vertebral body shape with reduced distance between the vertebral endplates.

Term Hierarchy

CClinical test,  RResearch test,  OOMIM,  GGeneReviews,  VClinVar  
  • CROGVBrachyolmia - Maroteaux type

Recent clinical studies

Etiology

Ürel-Demir G, Şimşek-Kiper PÖ, Öncel İ, Utine GE, Haliloğlu G, Boduroğlu K
Eur J Paediatr Neurol 2021 May;32:46-55. Epub 2021 Mar 16 doi: 10.1016/j.ejpn.2021.03.011. PMID: 33774370
Nishimura G, Lausch E, Savarirayan R, Shiba M, Spranger J, Zabel B, Ikegawa S, Superti-Furga A, Unger S
Am J Med Genet C Semin Med Genet 2012 Aug 15;160C(3):190-204. Epub 2012 Jul 12 doi: 10.1002/ajmg.c.31335. PMID: 22791502
Shohat M, Lachman R, Gruber HE, Rimoin DL
Am J Med Genet 1989 Jun;33(2):209-19. doi: 10.1002/ajmg.1320330214. PMID: 2669482

Diagnosis

Ürel-Demir G, Şimşek-Kiper PÖ, Öncel İ, Utine GE, Haliloğlu G, Boduroğlu K
Eur J Paediatr Neurol 2021 May;32:46-55. Epub 2021 Mar 16 doi: 10.1016/j.ejpn.2021.03.011. PMID: 33774370
Cho TJ, Matsumoto K, Fano V, Dai J, Kim OH, Chae JH, Yoo WJ, Tanaka Y, Matsui Y, Takigami I, Monges S, Zabel B, Shimizu K, Nishimura G, Lausch E, Ikegawa S
Am J Med Genet A 2012 Apr;158A(4):795-802. Epub 2012 Mar 14 doi: 10.1002/ajmg.a.35268. PMID: 22419508

Prognosis

Cho TJ, Matsumoto K, Fano V, Dai J, Kim OH, Chae JH, Yoo WJ, Tanaka Y, Matsui Y, Takigami I, Monges S, Zabel B, Shimizu K, Nishimura G, Lausch E, Ikegawa S
Am J Med Genet A 2012 Apr;158A(4):795-802. Epub 2012 Mar 14 doi: 10.1002/ajmg.a.35268. PMID: 22419508

Clinical prediction guides

Cho TJ, Matsumoto K, Fano V, Dai J, Kim OH, Chae JH, Yoo WJ, Tanaka Y, Matsui Y, Takigami I, Monges S, Zabel B, Shimizu K, Nishimura G, Lausch E, Ikegawa S
Am J Med Genet A 2012 Apr;158A(4):795-802. Epub 2012 Mar 14 doi: 10.1002/ajmg.a.35268. PMID: 22419508
Shohat M, Lachman R, Gruber HE, Rimoin DL
Am J Med Genet 1989 Jun;33(2):209-19. doi: 10.1002/ajmg.1320330214. PMID: 2669482

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