This syndrome is characterized by the association of global developmental delay, osteopenia and skin anomalies. To date, only three cases (two brothers and one unrelated girl) have been reported. Central nervous system anomalies manifest as poor lang

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syndrome de retard de développement-ostéopénie-anomalies ectodermiques

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A rare multiple malformation syndrome with characteristics of severe intrauterine growth retardation, severe microcephaly with a sloping forehead, severe ichthyosis (collodion baby type), and facial dysmorphism. Severe central nervous system defects

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syndrome de Neu-Laxova

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Malignant neoplasm of spinal cord, cranial nerves and other parts of central nervous system

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Tumeur maligne de la moelle épinière, des nerfs crâniens et d'autres parties du système nerveux central

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https://icd.who.int/browse10/2 (...) [HTML] [2018-01-01]

Others have searched : ondine syndrome ondine's curse posterior cord syndrome central cord syndrome complete cord syndrome congenital central alveolar hypoventilation congenital central hypoventilation syndrome idiopathic central alveolar hypoventilation sleep-induced apnea tethered cord syndrome

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'central cord syndrome' ->

Date index: 2021-11-18