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Rudimentary postaxial polydactyly of hands

MedGen UID:
870704
Concept ID:
C4025158
Congenital Abnormality
HPO: HP:0005676

Term Hierarchy

CClinical test,  RResearch test,  OOMIM,  GGeneReviews,  VClinVar  
  • CROGVRudimentary postaxial polydactyly of hands

Conditions with this feature

Pseudoaminopterin syndrome
MedGen UID:
163196
Concept ID:
C0795939
Disease or Syndrome
The pseudoaminopterin syndrome (aminopterin syndrome sine aminopterin; ASSA) is a multiple congenital anomaly disorder characterized by ossification defects of the skull, dysmorphic facial features, delayed development, and variable limb defects. The clinical features resemble the embryopathy caused by maternal treatment with the folic acid antagonist aminopterin, which has been recognized since 1952 (Thiersch, 1952) when aminopterin was used as an abortifacient. The characteristic phenotype of the children who survived infancy after having been exposed to aminopterin or its methyl derivative, methotrexate, in early pregnancy included a very unusual facies, skull anomalies, and skeletal defects (summary by Fraser et al., 1987).

Recent clinical studies

Etiology

Palencia-Campos A, Martínez-Fernández ML, Altunoglu U, Soto-Bielicka P, Torres A, Marín P, Aller E, Şentürk L, Berköz Ö, Yıldıran M, Kayserili H, Gil-Camarero E, Colli-Lista G, Sanchís-Calvo A, Carretero A; ECEMC Working Group on Polydactyly, Guillén-Navarro E, López-González V, Ballesta-Martínez M, Rosell J, Aglan MS, Temtamy S, Otaify GA, Cuevas-Catalina L, Torres-Saavedra MN, Nevado J, Tenorio J, Lapunzina P, Bermejo-Sánchez E, Ruiz-Pérez VL
Hum Mutat 2020 Jan;41(1):265-276. Epub 2019 Nov 6 doi: 10.1002/humu.23921. PMID: 31549748
Katz K, Linder N
J Pediatr Orthop 2011 Jun;31(4):448-9. doi: 10.1097/BPO.0b013e31821addb6. PMID: 21572283

Diagnosis

Palencia-Campos A, Martínez-Fernández ML, Altunoglu U, Soto-Bielicka P, Torres A, Marín P, Aller E, Şentürk L, Berköz Ö, Yıldıran M, Kayserili H, Gil-Camarero E, Colli-Lista G, Sanchís-Calvo A, Carretero A; ECEMC Working Group on Polydactyly, Guillén-Navarro E, López-González V, Ballesta-Martínez M, Rosell J, Aglan MS, Temtamy S, Otaify GA, Cuevas-Catalina L, Torres-Saavedra MN, Nevado J, Tenorio J, Lapunzina P, Bermejo-Sánchez E, Ruiz-Pérez VL
Hum Mutat 2020 Jan;41(1):265-276. Epub 2019 Nov 6 doi: 10.1002/humu.23921. PMID: 31549748
Ochi K, Horiuchi Y, Takayama S, Saito H
Hand Surg 2011;16(1):91-3. doi: 10.1142/S0218810411005138. PMID: 21348039

Therapy

Katz K, Linder N
J Pediatr Orthop 2011 Jun;31(4):448-9. doi: 10.1097/BPO.0b013e31821addb6. PMID: 21572283

Prognosis

Katz K, Linder N
J Pediatr Orthop 2011 Jun;31(4):448-9. doi: 10.1097/BPO.0b013e31821addb6. PMID: 21572283

Clinical prediction guides

Chen CP, Lin SP, Chen MR, Su JW, Chern SR, Chen YJ, Lee MS, Wang W
Genet Couns 2012;23(2):195-200. PMID: 22876577
Umm-e-Kalsoom, Basit S, Kamran-ul-Hassan Naqvi S, Ansar M, Ahmad W
Hum Genet 2012 Mar;131(3):415-22. Epub 2011 Aug 30 doi: 10.1007/s00439-011-1085-7. PMID: 21877132
Gesase AP
Ital J Anat Embryol 2006 Oct-Dec;111(4):179-86. PMID: 17385274
Zhao H, Tian Y, Breedveld G, Huang S, Zou Y, Y J, Chai J, Li H, Li M, Oostra BA, Lo WH, Heutink P
Eur J Hum Genet 2002 Mar;10(3):162-6. doi: 10.1038/sj.ejhg.5200790. PMID: 11973619

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