Tratamiento y desenlace obstétrico de una paciente con artrogriposis múltiple congénita

Guzmán-López, Abel; Treviño-Montemayor, Oscar Rubén; Soria-López, Juan Antonio; Saldivar-Rodríguez, Donato; López-Rodríguez, Julio César.
Ginecol. obstet. Méx ; 87(4): 253-256, ene. 2019.
Artículo en Español | LILACS-Express | ID: biblio-1250029

Documentos relacionados

  1. Fetal akinesia deformation sequence syndrome associated with recessive TTN variants.
  2. Fetal arthrogryposis-what do we tell the prospective parents?
  3. DST variants are responsible for neurogenic arthrogryposis multiplex congenita enlarging the spectrum of type VI hereditary sensory autonomic neuropathy.
  4. The emerging spectrum of fetal acetylcholine receptor antibody-related disorders (FARAD).
  5. Fetal arthrogryposis multiplex congenita/fetal akinesia deformation sequence (FADS)-Aetiology, diagnosis, and management.
  6. Clinical and molecular characteristics of 26 fetuses with lethal multiple congenital contractures.
  7. Fibrodysplasia ossificans progressiva in a 3-year-old female patient.
  8. Embryonic movement stimulates joint formation and development: Implications in arthrogryposis multiplex congenita.
  9. De novo mutations of <i>SCN1A</i> are responsible for arthrogryposis broadening the <i>SCN1A</i>-related phenotypes.
  10. Frequency and associated factors of non-adherence to prenatal care in pregnant women 35 years of age or older in Cauca, Colombia, 2016-2018