Results 201 to 210 of about 338,913 (237)
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Neonatal Hypotonia Following in Utero Exposure to Antidepressant Drugs
Journal of Pediatrics, 2022Associations between fetal exposure to antidepressants and neonatal hypotonia were studied using VigiBase and the French PharmacoVigilance Database. We identified significant associations between neonatal hypotonia and clomipramine, venlafaxine, and imipramine. Reports from the French database implicated prolonged fetal exposure. Neonatal hypotonia may
Fabian Guénolé +2 more
exaly +3 more sources
Neonatal Hypotonia: Don't Forget the Prader-Willi Syndrome
Acta Paediatrica, International Journal of Paediatrics, 2003During the neonatal period the diagnosis of the Prader‐Willi syndrome (PWS) is difficult because the syndrome is expressed mainly by severe hypotonia at this age and the typical clinical features of later life are not yet present. Aim: To identify all the PWS clinical markers in severe hypotonic newborns, which could facilitate an early diagnosis of ...
Andrea Corrias, L Bosio
exaly +5 more sources
Neonatal Hypotonia and Cardiomyopathy Secondary to Type IV Glycogenosis
Acta Neuropathologica, 1994A neonate with deficiency of branching enzyme (glycogenosis type IV) presented symptoms of severe hypotonia pre- and postnatally, and dilated cardiomyopathy in early infancy. The classical clinical manifestation of liver cirrhosis was not present, although amylopectin-like inclusions were found in the hepatocytes.
Mark L. Splaingard +2 more
exaly +5 more sources
Hypotonia in the Neonatal Intensive Care Unit
Clinics in PerinatologyHypotonia is a common presenting symptom in the neonatal intensive care unit (NICU). Hypotonia can be a manifestation of an underlying systemic illness, a primary nervous system disease, or a peripheral nervous system disease. Examination and history can suggest specific causes, but rapid and accurate diagnosis remains challenging due to the broad ...
Niranjana Natarajan +2 more
exaly +3 more sources
Apneic Crises: A Clue for MECP2 Testing in Severe Neonatal Hypotonia-Respiratory Failure
European Journal of Paediatric Neurology, 2012 Males with methyl-CpG-binding protein 2 (MECP2) mutations may present with neonatal encephalopathy. We report on an infant with a MECP2 mutation who exhibited complex constellation of symptoms, including severe hypotonia, respiratory failure, and apneic ...
Raffaele Falsaperla +2 more
exaly +3 more sources
Journal of Paediatrics and Child Health, 2017
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Bruno, Law-Ye, Catherine, Adamsbaum
openaire +4 more sources
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Bruno, Law-Ye, Catherine, Adamsbaum
openaire +4 more sources
Nederlands tijdschrift voor geneeskunde, 2020
Hypotonia in neonates is a relatively common symptom, and has a broad differential diagnosis. Despite advances in diagnostic techniques over the past few years, understanding where hypotonia in a neonate originates remains a challenge. Hypotonia can be a result of diseases of the central or peripheral nervous system; differentiation between a central ...
Robin Miralles, Deepa Panjwani
openaire +3 more sources
Hypotonia in neonates is a relatively common symptom, and has a broad differential diagnosis. Despite advances in diagnostic techniques over the past few years, understanding where hypotonia in a neonate originates remains a challenge. Hypotonia can be a result of diseases of the central or peripheral nervous system; differentiation between a central ...
Robin Miralles, Deepa Panjwani
openaire +3 more sources
Neuromuscular Disorders, 2009 International audienceNeonatal hypotonia is frequently observed with a highly variable clinical presentation. Congenital myopathies that are classically characterized by the presence of structural changes of the muscle fibres such as cores, rods and ...
Isabelle Marty +2 more
exaly +2 more sources
Seminars in Neurology, 1993
The approach to a newborn with hypotonia should not differ substantially from that to an older patient. The examination may be more difficult to interpret, especially in evaluating mental status and muscle strength. However, laboratory studies such as serum enzymes, EMG, and muscle biopsy may be very specific in helping the neurologist to arrive at a ...
V S, Miller, M, Delgado, S T, Iannaccone
openaire +2 more sources
The approach to a newborn with hypotonia should not differ substantially from that to an older patient. The examination may be more difficult to interpret, especially in evaluating mental status and muscle strength. However, laboratory studies such as serum enzymes, EMG, and muscle biopsy may be very specific in helping the neurologist to arrive at a ...
V S, Miller, M, Delgado, S T, Iannaccone
openaire +2 more sources