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Results for “FIBROUS DYSPLASIA OF BONE”

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At least 523 records · Page 29Linked to original sources
PubMed1989

[Type I pseudohypoparathyroidism. Study and prolonged follow-up of a case].

The prolonged evolution of a case of pseudohypoparathyroidism with hereditary osteodystrophy (AHO) and osteitis fibrosa is presented. The diagnosis was confirmed by the existence of a peculiar phenotype, hypocalcaemia, hyperphosphatemia, increased PTH values, and a lack of tubular response after PTH and radiological signs of hyperparathyroidism. The clinical and biochemical evolution, under 1.25 (OH)2D3 therapy with special emphasis on the growth and development were shown. The bibliography was also reviewed.

Child↗
PubMedDate not supplied

[Craniofacial polyostotic fibro-osseous dysplasia. (1) A clinical case].

Taking the opportunity of a richness of clinical and radiological manifestations from an uncommon pathology, the authors present a case on polyostotic bony--fibrous displasia with a large envelopment of the facial-skull massif, and outstand the role of the stomatologist as member of a multidisciplinary medical team and the successful therapheutical result achieved through the surgical intervention performed.

Adult↗
PubMed1979

Polyostotic fibrous dysplasia involving the maxilla and mandible: report of case.

The case presented here represents an aggressive form of polyostotic fibrous dysplasia. Because of lack of evidence to substantiate precocious puberty and abnormal pigmentation, Albright syndrome cannot be established. Because of the nature of this disease, its clinical course and prognosis are unpredictable. However, it is believed that continued growth of the lesion may necessitate additional surgery.

Child↗
PubMed1979

Congenital monostotic fibrous dysplasia--a new possibly autosomal recessive disorder.

Two siblings, a 3-month-old white male infant and a 12-day-old female infant, had an anterior mandibular bony lesion that, in both cases, had been present at birth. After evaluation of clinical, physical, radiographic, laboratory, and histologic findings, a diagnosis of congenital monostotic fibrous dysplasia was made. Thorough review of the literature on fibrous dysplasia yielded no similar cases. The two cases presented appear to be the first reported examples of congenital monostotic fibrous dysplasia in siblings. The parents said there was no consanguinity. The possibility of a new autosomal-recessive disorder is likely.

Chromosomes↗