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Distal arthrogryposis type 10(DA10)

MedGen UID:
349990
Concept ID:
C1861238
Disease or Syndrome
Synonyms: CONGENITAL PLANTAR CONTRACTURES; DA10; TENDO CALCANEUS, SHORT
SNOMED CT: Congenital plantar flexion contracture (1208482007); DA10 - distal arthrogryposis type 10 (1208482007); Distal arthrogryposis type 10 (1208482007)
Modes of inheritance:
Autosomal dominant inheritance
MedGen UID:
141047
Concept ID:
C0443147
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 heterozygotes. In the context of medical genetics, an autosomal dominant disorder is caused when a single copy of the mutant allele is present. Males and females are affected equally, and can both transmit the disorder with a risk of 50% for each child of inheriting the mutant allele.
 
Monarch Initiative: MONDO:0016675
OMIM®: 187370
Orphanet: ORPHA251515

Definition

A rare genetic distal arthrogryposis syndrome with characteristics of plantar flexion contractures typically presenting with toe-walking in infancy, variably associated with milder contractures of the hip, elbow, wrist and finger joints. No ocular or neurological abnormalities are associated and serum creatine phosphokinase levels are normal. [from SNOMEDCT_US]

Clinical features

From HPO
Talipes
MedGen UID:
220976
Concept ID:
C1301937
Congenital Abnormality
A deformity of foot and ankle that has different subtypes that are talipes equinovarus, talipes equinovalgus, talipes calcaneovarus and talipes calcaneovalgus.
Plantar flexion contracture
MedGen UID:
349991
Concept ID:
C1861239
Finding
A type of contracture in which the plantar flexion muscles are contracted.
Tip-toe gait
MedGen UID:
98104
Concept ID:
C0427144
Finding
An abnormal gait pattern characterized by the failure of the heel to contact the floor at the onset of stance during gait.
Distal arthrogryposis
MedGen UID:
120512
Concept ID:
C0265213
Disease or Syndrome
An inherited primary limb malformation disorder characterized by congenital contractures of two or more different body areas and without primary neurologic and/or muscle disease that affects limb function.
Elbow flexion contracture
MedGen UID:
98367
Concept ID:
C0409338
Acquired Abnormality
An elbow contracture that limits the ability of the elbow joint to be extended (straightened), meaning that the elbow is fixed in an flexed (bent) position.
Wrist flexion contracture
MedGen UID:
592338
Concept ID:
C0409345
Acquired Abnormality
A chronic loss of wrist joint motion due to structural changes in muscle, tendons, ligaments, or skin that prevent normal movement of the joints of the wrist.
Camptodactyly of finger
MedGen UID:
98041
Concept ID:
C0409348
Finding
The distal interphalangeal joint and/or the proximal interphalangeal joint of the fingers cannot be extended to 180 degrees by either active or passive extension.
Hamstring contractures
MedGen UID:
98375
Concept ID:
C0410266
Anatomical Abnormality
Elevated circulating creatine kinase concentration
MedGen UID:
69128
Concept ID:
C0241005
Finding
An elevation of the level of the enzyme creatine kinase (also known as creatine phosphokinase (CK; EC 2.7.3.2) in the blood. CK levels can be elevated in a number of clinical disorders such as myocardial infarction, rhabdomyolysis, and muscular dystrophy.

Recent clinical studies

Etiology

Oliwa A, Hendson G, Longman C, Synnes A, Seath K, Barnicoat A, Hall JG, Patel MS
Am J Med Genet A 2023 Feb;191(2):546-553. Epub 2022 Nov 1 doi: 10.1002/ajmg.a.63019. PMID: 36317804
Li Y, Nong T, Li Y, Li X, Li Z, Lv H, Xu H, Li J, Zhu M
Mol Genet Genomic Med 2022 Dec;10(12):e2042. Epub 2022 Sep 7 doi: 10.1002/mgg3.2042. PMID: 36069346Free PMC Article
Serra G, Antona V, Cannata C, Giuffrè M, Piro E, Schierz IAM, Corsello G
Ital J Pediatr 2022 Jul 29;48(1):133. doi: 10.1186/s13052-022-01329-z. PMID: 35906671Free PMC Article
Dahan-Oliel N, Collins J, Rauch D, Bukovy G, Hamdy R, Rauch F
Bone 2020 Aug;137:115454. Epub 2020 May 25 doi: 10.1016/j.bone.2020.115454. PMID: 32464275
Okubo M, Fujita A, Saito Y, Komaki H, Ishiyama A, Takeshita E, Kojima E, Koichihara R, Saito T, Nakagawa E, Sugai K, Yamazaki H, Kusaka K, Tanaka H, Miyake N, Matsumoto N, Sasaki M
Am J Med Genet A 2015 May;167A(5):1100-6. Epub 2015 Feb 25 doi: 10.1002/ajmg.a.36881. PMID: 25712306

Diagnosis

Oliwa A, Hendson G, Longman C, Synnes A, Seath K, Barnicoat A, Hall JG, Patel MS
Am J Med Genet A 2023 Feb;191(2):546-553. Epub 2022 Nov 1 doi: 10.1002/ajmg.a.63019. PMID: 36317804
Serra G, Antona V, Cannata C, Giuffrè M, Piro E, Schierz IAM, Corsello G
Ital J Pediatr 2022 Jul 29;48(1):133. doi: 10.1186/s13052-022-01329-z. PMID: 35906671Free PMC Article
Dahan-Oliel N, Collins J, Rauch D, Bukovy G, Hamdy R, Rauch F
Bone 2020 Aug;137:115454. Epub 2020 May 25 doi: 10.1016/j.bone.2020.115454. PMID: 32464275
Li S, You Y, Gao J, Mao B, Cao Y, Zhao X, Zhang X
BMC Med Genet 2018 Oct 3;19(1):179. doi: 10.1186/s12881-018-0692-8. PMID: 30285720Free PMC Article
Maltese G, Tan SV, Bruno E, Brackenridge A, Thomas S
Diabet Med 2018 Oct;35(10):1457-1459. doi: 10.1111/dme.13701. PMID: 29862581

Therapy

Greggi T, Lolli F, Di Silvestre M, Martikos K, Vommaro F, Maredi E, Giacomini S, Baioni A, Cioni A
Stud Health Technol Inform 2012;176:334-7. PMID: 22744523

Prognosis

Oliwa A, Hendson G, Longman C, Synnes A, Seath K, Barnicoat A, Hall JG, Patel MS
Am J Med Genet A 2023 Feb;191(2):546-553. Epub 2022 Nov 1 doi: 10.1002/ajmg.a.63019. PMID: 36317804
Williams MS, Elliott CG, Bamshad MJ
Am J Med Genet A 2007 Apr 1;143A(7):752-6. doi: 10.1002/ajmg.a.31648. PMID: 17345626

Clinical prediction guides

Dahan-Oliel N, Collins J, Rauch D, Bukovy G, Hamdy R, Rauch F
Bone 2020 Aug;137:115454. Epub 2020 May 25 doi: 10.1016/j.bone.2020.115454. PMID: 32464275
Pantera H, Hu B, Moiseev D, Dunham C, Rashid J, Moran JJ, Krentz K, Rubinstein CD, Won S, Li J, Svaren J
Hum Mol Genet 2020 Jun 27;29(10):1689-1699. doi: 10.1093/hmg/ddaa082. PMID: 32356557Free PMC Article
Li S, You Y, Gao J, Mao B, Cao Y, Zhao X, Zhang X
BMC Med Genet 2018 Oct 3;19(1):179. doi: 10.1186/s12881-018-0692-8. PMID: 30285720Free PMC Article
Williams MS, Elliott CG, Bamshad MJ
Am J Med Genet A 2007 Apr 1;143A(7):752-6. doi: 10.1002/ajmg.a.31648. PMID: 17345626

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