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Spondyloepiphyseal dysplasia tarda with characteristic facies

MedGen UID:
325071
Concept ID:
C1838653
Disease or Syndrome
Synonym: Spondyloepiphyseal Dysplasia Tarda with Characteristic Facies
 
Monarch Initiative: MONDO:0010815
OMIM®: 600093

Clinical features

From HPO
Flattened knee epiphyses
MedGen UID:
870696
Concept ID:
C4025150
Anatomical Abnormality
Global developmental delay
MedGen UID:
107838
Concept ID:
C0557874
Finding
A delay in the achievement of motor or mental milestones in the domains of development of a child, including motor skills, speech and language, cognitive skills, and social and emotional skills. This term should only be used to describe children younger than five years of age.
Spondyloepiphyseal dysplasia
MedGen UID:
20916
Concept ID:
C0038015
Finding
A disorder of bone growth affecting the vertebrae and the ends of the long bones (epiphyses).
Microcephaly
MedGen UID:
1644158
Concept ID:
C4551563
Finding
Head circumference below 2 standard deviations below the mean for age and gender.
Broad nasal tip
MedGen UID:
98424
Concept ID:
C0426429
Finding
Increase in width of the nasal tip.
Thick lower lip vermilion
MedGen UID:
326567
Concept ID:
C1839739
Finding
Increased thickness of the lower lip, leading to a prominent appearance of the lower lip. The height of the vermilion of the lower lip in the midline is more than 2 SD above the mean. Alternatively, an apparently increased height of the vermilion of the lower lip in the frontal view (subjective).
Thick upper lip vermilion
MedGen UID:
339521
Concept ID:
C1846423
Finding
Height of the vermilion of the upper lip in the midline more than 2 SD above the mean. Alternatively, an apparently increased height of the vermilion of the upper lip in the frontal view (subjective).
Wide nasal bridge
MedGen UID:
341441
Concept ID:
C1849367
Finding
Increased breadth of the nasal bridge (and with it, the nasal root).
Broad philtrum
MedGen UID:
344210
Concept ID:
C1854111
Finding
Distance between the philtral ridges, measured just above the vermilion border, more than 2 standard deviations above the mean, or alternatively, an apparently increased distance between the ridges of the philtrum.
Short philtrum
MedGen UID:
350006
Concept ID:
C1861324
Finding
Distance between nasal base and midline upper lip vermilion border more than 2 SD below the mean. Alternatively, an apparently decreased distance between nasal base and midline upper lip vermilion border.

Professional guidelines

PubMed

Boerkoel CF, O'Neill S, André JL, Benke PJ, Bogdanovíć R, Bulla M, Burguet A, Cockfield S, Cordeiro I, Ehrich JH, Fründ S, Geary DF, Ieshima A, Illies F, Joseph MW, Kaitila I, Lama G, Leheup B, Ludman MD, McLeod DR, Medeira A, Milford DV, Ormälä T, Rener-Primec Z, Santava A, Santos HG, Schmidt B, Smith GC, Spranger J, Zupancic N, Weksberg R
Eur J Pediatr 2000 Jan-Feb;159(1-2):1-7. doi: 10.1007/s004310050001. PMID: 10653321

Recent clinical studies

Etiology

Nijhuis WH, Verhoef M, Sakkers RJB
Eur J Med Genet 2023 Nov;66(11):104851. Epub 2023 Sep 25 doi: 10.1016/j.ejmg.2023.104851. PMID: 37758161
Grange DK, Roessler HI, McClenaghan C, Duran K, Shields K, Remedi MS, Knoers NVAM, Lee JM, Kirk EP, Scurr I, Smithson SF, Singh GK, van Haelst MM, Nichols CG, van Haaften G
Am J Med Genet C Semin Med Genet 2019 Dec;181(4):658-681. doi: 10.1002/ajmg.c.31753. PMID: 31828977Free PMC Article
Bober MB, Jackson AP
Curr Osteoporos Rep 2017 Apr;15(2):61-69. doi: 10.1007/s11914-017-0348-1. PMID: 28409412Free PMC Article
Wainwright H, Beighton P
Virchows Arch 2010 Dec;457(6):735-9. Epub 2010 Oct 5 doi: 10.1007/s00428-010-0982-9. PMID: 20922410
Howe AM, Lipson AH, Sheffield LJ, Haan EA, Halliday JL, Jenson F, David DJ, Webster WS
Am J Med Genet 1995 Sep 11;58(3):238-44. doi: 10.1002/ajmg.1320580309. PMID: 8533825

Diagnosis

Marques P, Korbonits M
Front Neuroendocrinol 2019 Jan;52:113-143. Epub 2018 Nov 15 doi: 10.1016/j.yfrne.2018.11.001. PMID: 30448536
Bober MB, Jackson AP
Curr Osteoporos Rep 2017 Apr;15(2):61-69. doi: 10.1007/s11914-017-0348-1. PMID: 28409412Free PMC Article
Faundes V, Castillo-Taucher S, Gonzalez-Hormazabal P, Chandler K, Crosby A, Chioza B
Eur J Med Genet 2014 Sep;57(9):536-42. Epub 2014 Jul 12 doi: 10.1016/j.ejmg.2014.07.001. PMID: 25019372
Chummun S, McLean NR, Nugent M, Anderson PJ, David DJ
J Craniofac Surg 2012 Jul;23(4):986-90. doi: 10.1097/SCS.0b013e31824e2683. PMID: 22777437
Marck PA, Kudryk WH
J Otolaryngol 1992 Apr;21(2):84-7. PMID: 1583713

Therapy

Gameiro J, Duarte I, Outerelo C, Lopes JA
J Bras Nefrol 2019 Apr-Jun;41(2):304-305. Epub 2019 Jan 21 doi: 10.1590/2175-8239-JBN-2018-0198. PMID: 30720853Free PMC Article
Wainwright H, Beighton P
Virchows Arch 2010 Dec;457(6):735-9. Epub 2010 Oct 5 doi: 10.1007/s00428-010-0982-9. PMID: 20922410
Monedero P, Garcia-Pedrajas F, Coca I, Fernandez-Liesa JI, Panadero A, de los Rios J
J Clin Anesth 1997 May;9(3):208-12. doi: 10.1016/s0952-8180(97)00033-0. PMID: 9172028
Howe AM, Lipson AH, Sheffield LJ, Haan EA, Halliday JL, Jenson F, David DJ, Webster WS
Am J Med Genet 1995 Sep 11;58(3):238-44. doi: 10.1002/ajmg.1320580309. PMID: 8533825
Sheffield LJ, Danks DM, Mayne V, Hutchinson AL
J Pediatr 1976 Dec;89(6):916-23. doi: 10.1016/s0022-3476(76)80596-3. PMID: 993917

Prognosis

Markova T, Kenis V, Melchenko E, Osipova D, Nagornova T, Orlova A, Zakharova E, Dadali E, Kutsev S
Genes (Basel) 2022 Jan 13;13(1) doi: 10.3390/genes13010137. PMID: 35052477Free PMC Article
Hochart A, Dieux A, Coucke P, Fron D, Fayoux P, Labalette P, Boutry N, Escande F, Aubert S, Renaud F, Rocourt N, Vinchon M, Leblond P
Am J Med Genet A 2015 Dec;167A(12):3204-8. Epub 2015 Sep 8 doi: 10.1002/ajmg.a.37361. PMID: 26345137
Faundes V, Castillo-Taucher S, Gonzalez-Hormazabal P, Chandler K, Crosby A, Chioza B
Eur J Med Genet 2014 Sep;57(9):536-42. Epub 2014 Jul 12 doi: 10.1016/j.ejmg.2014.07.001. PMID: 25019372
Langer R, Al-Gazali L, Raupp P, Varady E
Australas Radiol 2007 Jun;51(3):203-10. doi: 10.1111/j.1440-1673.2007.01714.x. PMID: 17504309
Boerkoel CF, O'Neill S, André JL, Benke PJ, Bogdanovíć R, Bulla M, Burguet A, Cockfield S, Cordeiro I, Ehrich JH, Fründ S, Geary DF, Ieshima A, Illies F, Joseph MW, Kaitila I, Lama G, Leheup B, Ludman MD, McLeod DR, Medeira A, Milford DV, Ormälä T, Rener-Primec Z, Santava A, Santos HG, Schmidt B, Smith GC, Spranger J, Zupancic N, Weksberg R
Eur J Pediatr 2000 Jan-Feb;159(1-2):1-7. doi: 10.1007/s004310050001. PMID: 10653321

Clinical prediction guides

Retrouvey JM, Taqi D, Tamimi F, Dagdeviren D, Glorieux FH, Lee B, Hazboun R, Krakow D, Sutton VR; Members of the BBD Consortium
Eur J Med Genet 2019 Dec;62(12):103606. Epub 2018 Dec 26 doi: 10.1016/j.ejmg.2018.12.011. PMID: 30593885Free PMC Article
Tuna EB, Koruyucu M, Kürklü E, Çifter M, Gençay K, Seymen F, Tüysüz B
J Craniomaxillofac Surg 2016 Aug;44(8):919-24. Epub 2016 Apr 26 doi: 10.1016/j.jcms.2016.04.025. PMID: 27325544
Krakow D, Cohn DH, Wilcox WR, Noh GJ, Raffel LJ, Sarukhanov A, Ivanova MH, Danielpour M, Grange DK, Elliott AM, Bernstein JA, Rimoin DL, Merrill AE, Lachman RS
Am J Med Genet A 2016 Oct;170(10):2652-61. Epub 2016 May 30 doi: 10.1002/ajmg.a.37772. PMID: 27240702Free PMC Article
Pichard DC, Boyce AM, Collins MT, Cowen EW
JAMA Dermatol 2014 Jul;150(7):760-3. doi: 10.1001/jamadermatol.2014.184. PMID: 24671640Free PMC Article
Wainwright H, Beighton P
Virchows Arch 2010 Dec;457(6):735-9. Epub 2010 Oct 5 doi: 10.1007/s00428-010-0982-9. PMID: 20922410

Recent systematic reviews

Hill M, Lewis C, Riddington M, Crowe B, DeVile C, Götherström C, Chitty L
Disabil Health J 2019 Jul;12(3):340-349. Epub 2018 Dec 31 doi: 10.1016/j.dhjo.2018.12.003. PMID: 30638886

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