Results 121 to 130 of about 708 (140)
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Congenital corneal opacification in De Barsy syndrome.
Archives of ophthalmology (Chicago, Ill. : 1960), 2001A newborn male was noted to have bilateral congenital corneal opacification. Findings from examination disclosed a variety of dysmorphic features, including cutis laxa, progeroid aspect, short stature, multiple hyperextensible subluxated joints, muscular hypotonia, and hyperreflexia.
A J, Aldave +4 more
openaire +1 more source
[De Barsy-Moens-Dierckx syndrome: unusual course in a neonate].
Klinische Padiatrie, 1995We report about a premature infant with a De Barsy-Moens-Dierckx-syndrome, which is a rare cutaneo-oculo-cerebral malformation-syndrome. It is defined by the combination of a progeroid aspect, cutis laxa, growth retardation, cornea clouding, mental retardation and athetoid movements. Furthermore, the reported case showed a remarkable thermolability and
M, Schierenberg +6 more
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De Barsy syndrome in an extreme preterm infant
2011We report a rare case of an extreme preterm infant with De Barsy syndrome characterized by severe mental retardation, cutis laxa, cloudy corneas, muscular hypotonia, and lax joints. The etiology of this syndrome is unknown but it is probably heterogeneous.
AL-SAGBAN, Heba +3 more
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Augenbefunde beim de Barsy-Syndrom
Klinische Monatsblätter für Augenheilkunde, 1985R. Rochels, M. Beck
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De Barsy syndrome type B presenting with cardiac and genitourinary abnormalities
Clinical Dysmorphology, 2016Atanu K, Dutta +4 more
openaire +2 more sources
Recent progress in Lynch syndrome and other familial colorectal cancer syndromes
Ca-A Cancer Journal for Clinicians, 2018Patrick M Boland +2 more
exaly
Clinical implications of de Barsy syndrome
Paediatric Anaesthesia, 2018Lindsay L Warner, Hugh M Smith
exaly

