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Multiple skeletal anomalies

MedGen UID:
870684
Concept ID:
C4025138
Finding
HPO: HP:0005775

Term Hierarchy

CClinical test,  RResearch test,  OOMIM,  GGeneReviews,  VClinVar  
  • CROGVMultiple skeletal anomalies

Conditions with this feature

Bailey-Bloch congenital myopathy
MedGen UID:
340586
Concept ID:
C1850625
Disease or Syndrome
STAC3 disorder is characterized by congenital myopathy, musculoskeletal involvement of the trunk and extremities, feeding difficulties, and delayed motor milestones. Most affected individuals have weakness with myopathic facies, scoliosis, kyphosis or kyphoscoliosis, and contractures. Other common findings are ptosis, abnormalities of the palate (including cleft palate), and short stature. Risk for malignant hyperthermia susceptibility and restrictive lung disease are increased. Intellect is typically normal. Originally described in individuals from the Lumbee Native American tribe (an admixture of Cheraw Indian, English, and African American ancestry) in the state of North Carolina and reported as Native American myopathy, STAC3 disorder has now been identified in numerous other populations worldwide.

Professional guidelines

PubMed

Spahiu L, Behluli E, Grajçevci-Uka V, Liehr T, Temaj G
J Mother Child 2022 Mar 1;26(1):118-123. Epub 2023 Feb 22 doi: 10.34763/jmotherandchild.20222601.d-22-00034. PMID: 36803942Free PMC Article
Padala SA, Barsouk A, Barsouk A, Rawla P, Vakiti A, Kolhe R, Kota V, Ajebo GH
Med Sci (Basel) 2021 Jan 20;9(1) doi: 10.3390/medsci9010003. PMID: 33498356Free PMC Article
Michels TC, Petersen KE
Am Fam Physician 2017 Mar 15;95(6):373-383. PMID: 28318212

Recent clinical studies

Etiology

Alatas I, Canaz H, Akkoyun N, Er A, Demirhan O, Kizilay D, Emel E
Pediatr Neurosurg 2015;50(2):57-62. Epub 2015 Mar 17 doi: 10.1159/000380770. PMID: 25792257
Riyaz N, Riyaz A, Chandran R, Rakesh SV
Indian J Dermatol Venereol Leprol 2005 Jul-Aug;71(4):279-81. doi: 10.4103/0378-6323.16624. PMID: 16394441

Diagnosis

Accogli A, Scala M, Calcagno A, Castello R, Torella A, Musacchia F, Allegri AME, Mancardi MM, Maghnie M, Severino M; Telethon Undiagnosed Diseases Program, Nigro V, Capra V
Am J Med Genet A 2018 Dec;176(12):2835-2840. Epub 2018 Sep 20 doi: 10.1002/ajmg.a.40534. PMID: 30238602
Durmaz CD, Evans G, Smith MJ, Ertop P, Akay BN, Tuncalı T
Cytogenet Genome Res 2018;154(2):57-61. Epub 2018 Mar 16 doi: 10.1159/000487747. PMID: 29544218
Sailani MR, Chappell J, Jingga I, Narasimha A, Zia A, Lynch JL, Mazrouei S, Bernstein JA, Aryani O, Snyder MP
Cold Spring Harb Mol Case Stud 2018 Feb;4(1) Epub 2018 Feb 1 doi: 10.1101/mcs.a001990. PMID: 29092958Free PMC Article
Castori M, Pascolini G, Parisi V, Sana ME, Novelli A, Nürnberg P, Iascone M, Grammatico P
Am J Med Genet A 2015 Apr;167A(4):842-51. Epub 2015 Feb 23 doi: 10.1002/ajmg.a.36983. PMID: 25708316
Maas SM, Kayserili H, Lam J, Apak MY, Hennekam RC
Am J Med Genet A 2004 Dec 1;131(2):127-33. doi: 10.1002/ajmg.a.30244. PMID: 15523657

Therapy

Addar MH
J Obstet Gynaecol Can 2004 Nov;26(11):1001-3. doi: 10.1016/s1701-2163(16)30422-4. PMID: 15560863
Ananov MV, Roginski VV, Yeolchijan SA, Reshetov IV
J Craniofac Surg 1996 Sep;7(5):358-62. doi: 10.1097/00001665-199609000-00008. PMID: 9133848

Prognosis

Sailani MR, Chappell J, Jingga I, Narasimha A, Zia A, Lynch JL, Mazrouei S, Bernstein JA, Aryani O, Snyder MP
Cold Spring Harb Mol Case Stud 2018 Feb;4(1) Epub 2018 Feb 1 doi: 10.1101/mcs.a001990. PMID: 29092958Free PMC Article
Dikoglu E, Simsek-Kiper PO, Utine GE, Campos-Xavier B, Boduroglu K, Bonafé L, Superti-Furga A, Unger S
Am J Med Genet A 2013 Dec;161A(12):3161-5. Epub 2013 Aug 16 doi: 10.1002/ajmg.a.36173. PMID: 24039145
Dundar M, Saatci C, Tasdemir S, Akcakus M, Caglayan AO, Ozkul Y
Eur J Med Genet 2009 Jul-Aug;52(4):247-9. Epub 2009 Mar 19 doi: 10.1016/j.ejmg.2009.03.005. PMID: 19303467
Riyaz N, Riyaz A, Chandran R, Rakesh SV
Indian J Dermatol Venereol Leprol 2005 Jul-Aug;71(4):279-81. doi: 10.4103/0378-6323.16624. PMID: 16394441
Albano LM, Sakae PP, Mataloun MM, Leone CR, Bertola DR, Kim CA
Rev Hosp Clin Fac Med Sao Paulo 2004 Apr;59(2):89-92. Epub 2004 Apr 26 doi: 10.1590/s0041-87812004000200008. PMID: 15122424

Clinical prediction guides

Wu J, Yang Y, He Y, Li Q, Wang X, Sun C, Wang L, An Y, Luo F
Hum Genomics 2019 Dec 5;13(1):63. doi: 10.1186/s40246-019-0238-y. PMID: 31806011Free PMC Article
Sailani MR, Chappell J, Jingga I, Narasimha A, Zia A, Lynch JL, Mazrouei S, Bernstein JA, Aryani O, Snyder MP
Cold Spring Harb Mol Case Stud 2018 Feb;4(1) Epub 2018 Feb 1 doi: 10.1101/mcs.a001990. PMID: 29092958Free PMC Article
Dikoglu E, Simsek-Kiper PO, Utine GE, Campos-Xavier B, Boduroglu K, Bonafé L, Superti-Furga A, Unger S
Am J Med Genet A 2013 Dec;161A(12):3161-5. Epub 2013 Aug 16 doi: 10.1002/ajmg.a.36173. PMID: 24039145
Laue K, Pogoda HM, Daniel PB, van Haeringen A, Alanay Y, von Ameln S, Rachwalski M, Morgan T, Gray MJ, Breuning MH, Sawyer GM, Sutherland-Smith AJ, Nikkels PG, Kubisch C, Bloch W, Wollnik B, Hammerschmidt M, Robertson SP
Am J Hum Genet 2011 Nov 11;89(5):595-606. Epub 2011 Oct 20 doi: 10.1016/j.ajhg.2011.09.015. PMID: 22019272Free PMC Article
Malhotra A, Pateman A, Chalmers R, Coman D, Menahem S
Fetal Diagn Ther 2009;25(1):54-7. Epub 2009 Jan 29 doi: 10.1159/000196816. PMID: 19176971

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