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  • Seckel syndrome Relevant markers:
    Beaked noseMicrognathia/retrognathiaSevere IUGR/SGA
    Parents markers:
    MicrocephalyFaceIntrauterine growth retardation (IUGR/SGA/FGR)
      Incidence:1/1000000 — -
      Involved genes:
      (gene — definition — chromosome)      		SCKL1 — 3q22.1-q24, SCKL2 — 18p11.31-q11.2, CEP152 — 15q21.1, CENPJ — 13q12.12, SCKL3 — 14q21-q22
      Inheritance mode:AR
      Other online databases:OrphaNet, OMIM, Geneva Foundation, Jablonski's Database
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