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A Case Report of Mega Cisterna Magna with Extra-cranial Features of Dandy-Walker Malformation in an Adult: Implications for the Dandy-Walker Complex Continuum. [PDF]
Balmores EJF.
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Hypertelorism in Neurofibromatosis
Neuropediatrics, 1986In eight out of thirty-four patients with neurofibromatosis hypertelorism was seen. This hypertelorism was diagnosed by measuring the intercanthal distance and calculating the interpupillary distance from it. The high incidence of hypertelorism in our group of patients (24%) makes its direct association with neurofibromatosis feasible.
E C, Wolters +3 more
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Tessier Clefts and Hypertelorism
Facial Plastic Surgery Clinics of North America, 2016Tessier's classification system for rare craniofacial clefts remains the most widely used today. It denotes the position of the cleft process in a schema based around the orbit, and facilitates communication between surgeons regarding these complicated conditions.
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Hypertelorism is probably more common than reports indicate, and many readers may recall characteristic facies in their clinical experience. Reported cases are, however, rare. I have found only thirteen cases in the literature and hence am reporting four recently observed in the pediatric service of the University of California. In 1890, Fridolin 1 of
WILLIAM ANTHONY REILLY
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The hypertelorism—hypospadias syndrome
Clinical Genetics, 1983An affected family (five cases and one questionable case) with the hypertelorism‐hypospadias syndrome is reported. Inheritance is either autosomal or X‐linked dominant.
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Hypertelorism and Orofacial Clefting Revisited: An Anthropometric Investigation
Objective: Since the 1960s, multiple studies have reported a tendency toward hypertelorism in individuals with nonsyndromic orofacial clefts (OFCs).
Seth M Weinberg +2 more
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Familial hypertelorism, characterized by widely spaced eyes, classically shows autosomal dominant inheritance (Teebi type), but some pedigrees are compatible with X-linkage.
Christian Babbs +2 more
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