Results 321 to 330 of about 145,893 (342)
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Pediatric Dermatology, 1962
Three patients having a remarkable congenital decrease in the connective tissues of the skin have been reported under the title of focal dermal hypoplasia. This defect appears as linear areas of thinning of the skin and herniations of adipose tissue in the form of yellowish papules.
R W, GOLTZ +3 more
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Three patients having a remarkable congenital decrease in the connective tissues of the skin have been reported under the title of focal dermal hypoplasia. This defect appears as linear areas of thinning of the skin and herniations of adipose tissue in the form of yellowish papules.
R W, GOLTZ +3 more
openaire +3 more sources
Dermatology, 1974
The case of an 11-year-old girl with typical symptoms of focal dermal hypoplasia (Goltz-Gorlin syndrome) is reported. In a mentally normal child a mild body asymmetry with ocular, skin, dental, and skeletal changes, more pronounced on the right side, has been detected.
L, Zergollern +3 more
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The case of an 11-year-old girl with typical symptoms of focal dermal hypoplasia (Goltz-Gorlin syndrome) is reported. In a mentally normal child a mild body asymmetry with ocular, skin, dental, and skeletal changes, more pronounced on the right side, has been detected.
L, Zergollern +3 more
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Journal of Pediatric Surgery, 1973
Summary Eight infants with extrahepatic biliary duct hypoplasia have been followed for periods ranging from 9 mo to 8 yr. Two have died. Although there may be a temporary clinical improvement following operative cholangiogram, the long-term prognosis is poor in patients with biliary duct hypoplasia.
S M, Krant, O, Swenson
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Summary Eight infants with extrahepatic biliary duct hypoplasia have been followed for periods ranging from 9 mo to 8 yr. Two have died. Although there may be a temporary clinical improvement following operative cholangiogram, the long-term prognosis is poor in patients with biliary duct hypoplasia.
S M, Krant, O, Swenson
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American Journal of Medical Genetics Part A, 2009
AbstractOdontoid hypoplasia is a developmental abnormality, which is often asymptomatic. However significant sequelae can occur in some individuals, particularly after head or neck trauma. This anomaly is not generally known to be familial. We report on four affected individuals in the same family with odontoid hypoplasia, suggesting autosomal dominant
Cathy A, Stevens +2 more
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AbstractOdontoid hypoplasia is a developmental abnormality, which is often asymptomatic. However significant sequelae can occur in some individuals, particularly after head or neck trauma. This anomaly is not generally known to be familial. We report on four affected individuals in the same family with odontoid hypoplasia, suggesting autosomal dominant
Cathy A, Stevens +2 more
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European Radiology, 1998
A case of bilateral glenoid hypoplasia in a boy afflicted with posterior fossa medulloblastoma is described. Glenoid hypoplasia is a rarely reported bilateral finding either in subjects complaining of shoulder pain or abduction/adduction movements reduction as well as shoulder recurrent dislocations.
G, Beluffi, P, Fiori, C, Rodino
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A case of bilateral glenoid hypoplasia in a boy afflicted with posterior fossa medulloblastoma is described. Glenoid hypoplasia is a rarely reported bilateral finding either in subjects complaining of shoulder pain or abduction/adduction movements reduction as well as shoulder recurrent dislocations.
G, Beluffi, P, Fiori, C, Rodino
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American Journal of Ophthalmology, 1970
Although recognized as early as 1915, hypoplasia of the optic nerve is reported as rel atively rare." Review of the English litera ture reveals 16 unilateral and 12 bilateral cases. The largest series was comprised of six cases and was reported by Whinery and Blodi.
W C, Edwards, W E, Layden
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Although recognized as early as 1915, hypoplasia of the optic nerve is reported as rel atively rare." Review of the English litera ture reveals 16 unilateral and 12 bilateral cases. The largest series was comprised of six cases and was reported by Whinery and Blodi.
W C, Edwards, W E, Layden
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The Journal of Laryngology & Otology, 1971
Focal dermal hypoplasia syndrome (fdh) is a congenital disorder of mesodermal derivation with some ectodermal participation. The disorder, first described in 1962, is characterized by tenacious defects consisting of thinning of the skin; herniations of adipose tissue; abnormal skin pigmentation and other skeletal, dental, ocular, hair, and nail ...
I W, Mair, C, Hoy
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Focal dermal hypoplasia syndrome (fdh) is a congenital disorder of mesodermal derivation with some ectodermal participation. The disorder, first described in 1962, is characterized by tenacious defects consisting of thinning of the skin; herniations of adipose tissue; abnormal skin pigmentation and other skeletal, dental, ocular, hair, and nail ...
I W, Mair, C, Hoy
openaire +2 more sources
Journal of Bronchology & Interventional Pulmonology, 2010
Patricia Mejía, Lozano +1 more
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Patricia Mejía, Lozano +1 more
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