A syndrome of benign congenital hypotonia, gross obesity, delayed intellectual development, retarded bone age, and unusual facies.
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Age Determination by Skeleton↗
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Results for “Facies”
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[Proceedings: Prosopitis perstans (facies leontina) as a special form of Melkersson-Rosenthal syndrome].
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Edema↗
[On a case of aortic supravalvular stenosis, elfish facies and mental deficiency. So-called Beuren's syndrome].
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Abnormalities, Multiple↗
Pediatric radiologic notes. Case no. 376. Larsen's syndrome (multiple congenital dislocations with characteristic facies).
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Abnormalities, Multiple↗
Use of fallout cesium-137 as a tracer to define the recent deltaic facies of a river.
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Cesium Isotopes↗
A familial syndrome of unusual facies associated with malocclusion and short stature.
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Adolescent↗
[Clinical electroencephalographic correlations in arachnoiditis of the facies superolateralis cerebri].
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Adolescent↗
Familial 'hypercalcaemia' facies with other unusual features and normal serum calcium in two brothers.
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Calcium↗
[Mental development of "muslims" (peculiar facies of concentration camp inmates in their terminal phase)].
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Emaciation↗
[On an unusual syndrome of supravalvular aortic stenosis, mental retardation and hypercalcemic facies].
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Aorta↗
[Larsen's syndrome: congenital dislocation of the knees and other joints, distinctive facies, and, frequently, cleft palate].
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Abnormalities, Multiple↗
Unusual facies, joint hypermobility, genital anomaly and short stature: a new dysmorphic syndrome.
Three brothers with a previously unrecognized pattern of malformations are presented. The syndrome is characterized by short stature; a broad, prominent forehead, hypertelorism, congenital ptosis, a broad, short nose with anteverted nostrils, a long, broad upper lip, low-set, abnormally shaped and posteriorly rotated ears; simian palmar creases; brachyclinodactyly; short fingers; ligamentous laxity allowing for hyperextensibility of the fingers, genu recurvatum, flat feet; and an anomalous penoscrotal configuration resulting in "saddle" deformity with scrotal folds incircling the base of the penis. This disorder is apparently transmitted as an X-linked recessive trait. It is important to recognize this syndrome because of its heritability and for prevention of neurologic problems consequent to ligamentous laxity and malformation of cervical vertebras.
Child↗
A new autosomal dominant syndrome of hypohidrotic ectodermal dysplasia and unusual facies.
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Adult↗
Dysmorphic facies, omphalocele, laryngeal and pharyngeal hypoplasia, spinal anomalies, and learning disabilities in a new dominant malformation syndrome.
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Adult↗
[Post-valvular pulmonary and aortic stenoses with unusual facies and mental retardation].
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Adolescent↗
[The stress of human hip joint. 3. The form of facies lunata].
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Acetabulum↗
Prima facie tort and physician countersuits.
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Humans↗
[Idiopathic hypercalcemia facies and unilateral segmentary hypoplasia of the kidney].
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Angiography↗