Disease group (age related)

Articles

• neonatal digestive polyposis
  6 April 2005

  Types
  hamartomatous Peutz-Jeghers polyp (#7776109#) Peutz-Jeghers syndrome (#7776109#)
  References
  Fernandez Seara MJ, Martinez Soto MI, Fernandez Lorenzo JR, Trabazo S, Gamborino E, Forteza Vila J. Peutz-Jeghers syndrome in a neonate. J Pediatr. 1995 Jun;126(6):965-7. PMID: #7776109#

• fetal respiratory diseases
  6 April 2004

  Diseases
  respiratory developmental anomalies
  disorders of the transition to extrauterine life
  perinatal pneumonia
  Lesional syndromes and lesions
  amniotic aspiration
  meconium aspiration
  pulmonary hemorrhage

• congenital myopathies
  20 March 2005

  Congenital myopathies are clinical and genetic heterogeneous disorders characterized by skeletal muscle weakness ranging in severity.
  Three major forms have been identified:
  actin myopathy
  intranuclear rod myopathy
  nemaline myopathy.
  Nemaline myopathy is the most common of these myopathies and is further subdivided into seven groups according to severity, progressiveness, and age of onset.
  At present, five genes have been linked to congenital myopathies.
  alpha-actin (ACTA1) (...)

• fetal tumors
  15 June 2004

  neonatl tumors