Results 261 to 270 of about 97,105 (315)
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Journal of Craniofacial Surgery, 2009
Asymmetric velopharyngeal incompetence (VPI) has a diverse etiology, but those without any underlying cleft, hemifacial microsomia (HFM), or facial asymmetry are rarely encountered. Such cases have been reported within the last few years, with unilateral velopharyngeal hypoplasia identified to be the underlying abnormality in these patients.
Ying-Chien, Tan, Philip Kuo-Ting, Chen
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Asymmetric velopharyngeal incompetence (VPI) has a diverse etiology, but those without any underlying cleft, hemifacial microsomia (HFM), or facial asymmetry are rarely encountered. Such cases have been reported within the last few years, with unilateral velopharyngeal hypoplasia identified to be the underlying abnormality in these patients.
Ying-Chien, Tan, Philip Kuo-Ting, Chen
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Clinical Orthopaedics and Related Research, 1977
Fibular hypoplasia occurs in differing degrees of severity with fibular hemimelia as its most severe form. Normally the distal epiphyseal plate of the fibula is at the same level as the distal end of the distal tibial epiphysis, whereas the tip of the proximal fibular epiphysis is level with the proximal tibial epiphyseal plate.
W H, Bohne, L, Root
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Fibular hypoplasia occurs in differing degrees of severity with fibular hemimelia as its most severe form. Normally the distal epiphyseal plate of the fibula is at the same level as the distal end of the distal tibial epiphysis, whereas the tip of the proximal fibular epiphysis is level with the proximal tibial epiphyseal plate.
W H, Bohne, L, Root
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The Journal of Hand Surgery, 2013
Thumb hypoplasia, congenital underdevelopment of the thumb, can range from a slight decrease in thumb size to complete absence of the thumb. As part of the radial longitudinal deficiency spectrum, other organ systems may be affected as well. Hence, the global health of the child should be addressed before focusing on the thumb.
Francisco, Soldado +2 more
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Thumb hypoplasia, congenital underdevelopment of the thumb, can range from a slight decrease in thumb size to complete absence of the thumb. As part of the radial longitudinal deficiency spectrum, other organ systems may be affected as well. Hence, the global health of the child should be addressed before focusing on the thumb.
Francisco, Soldado +2 more
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The British Journal of Radiology, 1983
From a randomised series of 500 adult patients, average measurements of the normal adult odontoid peg in the vertical and sagittal planes as seen on a standard lateral film of the cervical spine are given, and it is suggested that measurements which fall below this range should be interpreted as indicating "odontoid hypoplasia" irrespective of the ...
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From a randomised series of 500 adult patients, average measurements of the normal adult odontoid peg in the vertical and sagittal planes as seen on a standard lateral film of the cervical spine are given, and it is suggested that measurements which fall below this range should be interpreted as indicating "odontoid hypoplasia" irrespective of the ...
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The Journal of Hand Surgery, 2009
Hypoplasia of the thumb refers to a spectrum of clinical abnormalities ranging from a slightly small digit to complete absence (or aplasia) of the thumb unit. As a component of radial dysplasia, thumb hypoplasia can be either an isolated entity or seen in conjunction with other elements of radial longitudinal deficiency.
Scott A, Riley, Ronald C, Burgess
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Hypoplasia of the thumb refers to a spectrum of clinical abnormalities ranging from a slightly small digit to complete absence (or aplasia) of the thumb unit. As a component of radial dysplasia, thumb hypoplasia can be either an isolated entity or seen in conjunction with other elements of radial longitudinal deficiency.
Scott A, Riley, Ronald C, Burgess
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Endocrinology and Metabolism Clinics of North America, 2017
This article summarizes pituitary development and function as well as specific mutations of genes encoding the following transcription factors: HESX1, LHX3, LHX4, POU1F1, PROP1, and OTX2. Although several additional genetic defects related to hypopituitarism have been identified, this article focuses on these selected factors, as they have been well ...
Mariam, Gangat, Sally, Radovick
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This article summarizes pituitary development and function as well as specific mutations of genes encoding the following transcription factors: HESX1, LHX3, LHX4, POU1F1, PROP1, and OTX2. Although several additional genetic defects related to hypopituitarism have been identified, this article focuses on these selected factors, as they have been well ...
Mariam, Gangat, Sally, Radovick
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Clinics in Plastic Surgery, 1989
Maxillary hypoplasia and retrusion is complex. It may involve the dentoalveolar area, or it may involve the whole midface. It may be difficult to recognize, since the patient may come only with the complaint of nasal deformity, and the occlusion may be normal.
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Maxillary hypoplasia and retrusion is complex. It may involve the dentoalveolar area, or it may involve the whole midface. It may be difficult to recognize, since the patient may come only with the complaint of nasal deformity, and the occlusion may be normal.
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The Neuroradiology Journal, 2012
A rare case of segmental hypoplasia of the basilar artery is described in a 49-year-old man with transient vertebrobasilar ischemia, explored by magnetic resonance imaging (MRI) and digital angiography (DA). The embryology, clinical relevance and magnetic resonance findings of this arterial anomaly are discussed, with a review of six previously ...
CARANCI, Ferdinando +5 more
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A rare case of segmental hypoplasia of the basilar artery is described in a 49-year-old man with transient vertebrobasilar ischemia, explored by magnetic resonance imaging (MRI) and digital angiography (DA). The embryology, clinical relevance and magnetic resonance findings of this arterial anomaly are discussed, with a review of six previously ...
CARANCI, Ferdinando +5 more
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Seminars in Fetal and Neonatal Medicine, 2017
To survive the transition to extrauterine life, newborn infants must have lungs that provide an adequate surface area and volume to allow for gas exchange. The dynamic activities of fetal breathing movements and accumulation of lung luminal fluid are key to fetal lung development throughout the various phases of lung development and growth, first by ...
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To survive the transition to extrauterine life, newborn infants must have lungs that provide an adequate surface area and volume to allow for gas exchange. The dynamic activities of fetal breathing movements and accumulation of lung luminal fluid are key to fetal lung development throughout the various phases of lung development and growth, first by ...
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Focal dermal hypoplasia without focal dermal hypoplasia
American Journal of Medical Genetics Part A, 2013Focal dermal hypoplasia (FDH; Goltz–Gorlin syndrome) is an X‐linked dominant disorder affecting mainly tissues of ectodermal and mesodermal origin. The phenotype is characterized by hypoplastic linear skin lesions, eye malformations, hair and teeth anomalies, and multiple limbs malformations. The disorder is caused by PORCN mutations.
Contreras-Capetillo, Silvina N. +3 more
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