Results 191 to 200 of about 339,801 (231)
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Cerebro-oculofacio-skeletal Syndrome
Archives of Pediatrics & Adolescent Medicine, 1977Sir .—An article by Preus et al ( Am J Dis Child 131:62, 1977) describes a syndrome of skeletal, facial, and ocular anomalies, microcephaly, intrauterine growth retardation, and hypotonia in two infants associated with renal anomalies and oligohydramnios. The authors have attributed these features to the cerebrooculofacio-skeletal syndrome.
A D, Mease, G B, Merestein
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Cerebro-costo-mandibular syndrome
American Journal of Medical Genetics, 1996We describe two boys with the cerebro-costo-mandibular syndrome (CCMS). Both patients presented with Pierre Robin anomaly and respiratory insufficiency and died 12 hours and 10 months after birth. The first boy had muscular hypotonia, severe micrognathia, glossoptosis, short palate, preauricular tag, paraumbilical fibroma, and a small and narrow thorax.
Plotz, FB +3 more
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Cerebro‐Costo‐Mandibular Syndrome
Australasian Radiology, 1992ABSTRACTCerebro‐costo‐mandibular syndrome (CCM) is a very rare entity with oro‐facial features closely resembling Pierre‐Robin anomaly (1,2). We describe a patient with typical features: severe micro‐gnathia, glossoptosis, central cleft soft palate and multiple posterior rib‐gap defects Seen on chest radiograph.
C T, Lim, M T, Koh
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2017
Definir "adolescencia" es algo bastante difícil, al punto que cada uno de nosotros tiene una idea diferente al respecto, incluyendo maestros, padres/madres y hasta los propios adolescentes. En este contexto, la psicología y las neurociencias aportan elementos que nos pueden ayudar a armar el rompecabezas que representa un adolescente.
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Definir "adolescencia" es algo bastante difícil, al punto que cada uno de nosotros tiene una idea diferente al respecto, incluyendo maestros, padres/madres y hasta los propios adolescentes. En este contexto, la psicología y las neurociencias aportan elementos que nos pueden ayudar a armar el rompecabezas que representa un adolescente.
openaire +1 more source

