article
INTERMITTENT MUSCULAR WEAKNESS, EXTRASYSTOLES, AND MULTIPLE DEVELOPMENTAL ANOMALIES
Acta Paediatrica · 1971 · Vol. 60(5) · pp. 559–564
Ellen Damgaard Andersen✉(Copenhagen University Hospital)Peter A. Krasilnikoff(Copenhagen University Hospital)HANS OVERVAD(Copenhagen University Hospital)
Abstract
Summary A description is given of an eight‐year‐old boy with extrasystoles, seizures of muscular weakness, and multiple developmental anomalies (dwarfism, scaphocephalic skull, hypertelorism, bilateral ptosis, low‐set ears, broad nose, mandibular hypoplasia, aplasia of a number of teeth, defect of both the soft and osseous palate, inward bending of the fifth fingers, single transverse palmar crease of both hands, and cryptorchidism). These findings suggest a specific syndrome, but no similar description was found in the literature. The investigations disclosed no signs of either a chromosomal, a neuromuscular, or an endocrine disease.
Genetics and Neurodevelopmental DisordersNeurogenetic and Muscular Disorders ResearchGenomic variations and chromosomal abnormalitiesMedicineHypertelorismHypoplasiaPtosisAplasiaWeaknessAnatomySkullPediatricsSurgery
MeSH terms
Abnormalities, MultipleAnodontiaBlepharoptosisChildCleft PalateCleidocranial DysplasiaCraniofacial DysostosisDwarfismEar, ExternalElectrocardiographyCardiac Complexes, PrematureHand Deformities, CongenitalHeart Septal Defects, VentricularHumansMale
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References
FAMILIAL HEART DISEASE WITH SKELETAL MALFORMATIONS
Heart · 1960 · 503 citations
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