La enfermedad de Steinert es una rara miopatía hereditaria caracterizada por debilidad muscular generalizada, miotonía y afección multisistémica. Aunque los . Download Citation on ResearchGate | Distrofia miotónica de Steinert | The complexity and variability of the manifestations of myotonic. Distrofia miotónica o enfermedad de Steinert: estudio clínico-histopatológico de tres casos de una família. Arq. Neuro-Psiquiatr. [online]. , vol, n

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Myotonic dystrophy is an unusual entity, which is rarely associated with pregnancy dietrofia to the fact that those people who are affected usually present with genital atrophy and hypogonadism. Its association with pregnancy can lead to different problems.

The myotony often worsens and obstetric complications increase; miscarriage, preterm delivery, hydrops fetalis, intrauterine death, difficulties in expulsion, intra and post partum haemorrhage.

Signs of fetal affectation during pregnancy are eistrofia, hydramnios, a sfeinert in fetal movements, and a slow fetal heart rate. Familial antecedents, severe hypotony or respiratory distress in the neonate are suggestive of the congenital form of myotonic dystrophy. The congenital form has a poor prognosis, and is more difficult to diagnose.

Today, molecular steinnert techniques allow to make both prenatal and an early neonatal diagnosis. Barber aI. Eguiluz aW. Plasencia aO. Hospital Universitario Materno-Infantil de Canarias. Las Palmas de Gran Canaria. Today, molecular genetic techniques allow to make both prenatal and an early neonatal diagnosis.

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Distrofia miotónica de steinert y gestación | Clínica e Investigación en Ginecología y Obstetricia

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