AI Article Synopsis

  • - The identification of a shared cause for MASA syndrome and X-linked hydrocephalus has led to improved diagnosis of these previously separate neurological disorders.
  • - A male fetus was diagnosed with MASA syndrome at 29 weeks of gestation by observing signs like hydrocephalus and underdeveloped corpus callosum.
  • - The family history indicated a 25% risk of the fetus being affected, and while prenatal diagnosis was made via ultrasound, molecular confirmation was completed post-birth.

Article Abstract

The recent identification of a common etiology among MASA syndrome (McKusick 303300), X-linked hydrocephalus (HSAS) (McKusick 307000) and other related neurological disorders, which had previously been considered distinct nosological entities, allowed us to diagnose MASA syndrome in a male fetus in a primigravida at the 29th week of gestation by sonographic signs of the MASA spectrum such as hydrocephalus and hypoplasia of corpus callosum. Indeed, the evidence of an X-linked neurological disease in the brother and the maternal uncle of the pregnant women enabled us to estimate a 25% risk of a male fetus being an affected hemizygote. The way in which a prenatal diagnosis, based on instrumental procedures, was reached is described since the authors were unable to perform, at the time of the observation, a molecular confirmation which was carried out only after birth.

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Source
http://dx.doi.org/10.1002/1097-0223(200012)20:12<1012::aid-pd963>3.0.co;2-xDOI Listing

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