Results 161 to 170 of about 12,560 (202)

Apert Syndrome. [PDF]

open access: yesIndian Dermatol Online J
Gupta P, Sangwan P, Thakur V.
europepmc   +1 more source
Some of the next articles are maybe not open access.

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Hypertelorism in Neurofibromatosis

Neuropediatrics, 1986
In 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
exaly   +3 more sources

Tessier Clefts and Hypertelorism

Facial Plastic Surgery Clinics of North America, 2016
Tessier'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.
exaly   +3 more sources

HYPERTELORISM

open access: yesJournal of the American Medical Association, 1931
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
openaire   +2 more sources

The hypertelorism—hypospadias syndrome

Clinical Genetics, 1983
An affected family (five cases and one questionable case) with the hypertelorism‐hypospadias syndrome is reported. Inheritance is either autosomal or X‐linked dominant.
exaly   +3 more sources

Hypertelorism and Orofacial Clefting Revisited: An Anthropometric Investigation

open access: yesCleft Palate-Craniofacial Journal, 2017
Objective: Since the 1960s, multiple studies have reported a tendency toward hypertelorism in individuals with nonsyndromic orofacial clefts (OFCs).
Seth M Weinberg   +2 more
exaly   +2 more sources

Duplication of theEFNB1gene in familial hypertelorism: imbalance in ephrin‐B1 expression and abnormal phenotypes in humans and mice

open access: yesHuman Mutation, 2011
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
exaly   +2 more sources

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