Descriptor: "Osteoma genetics" / Language: french - Searchworks@Jio Institute Digital Library Search Results

Author: Camuzard JF, Vaille G, Santini J, Raspaldo H, and Demard F
Subjects: Adolescent, Adult, Epidermal Cyst genetics, Female, Gardner Syndrome complications, Humans, Lipoma genetics, Male, Mandibular Neoplasms genetics, Pedigree, Tooth Abnormalities genetics, Gardner Syndrome genetics, Osteoma genetics, Skull Neoplasms genetics
Abstract: Through a family form study and a literature review, the authors define the symptoms of the Gardner's disease and the checkup to be carried out. Sometimes, the surgical treatment, proposed in an aesthetical purpose, is difficult to carry out due to the tumor location and consistency. Incomplete forms are likely to be more frequent but the risk of colic degeneration remains the same as for the usual form. Examination and multi-departmental care are required.
Published: 1990

Author: Renier JC and François H
Subjects: Adolescent, Adult, Child, Child, Preschool, Female, Humans, Male, Middle Aged, Osteoma pathology, Pedigree, Skin Neoplasms pathology, Osteoma genetics, Skin Neoplasms genetics
Published: 1980

Author: Lorette G, Valat JP, Gatti P, Fetissoff F, Arbeille B, Boistard C, and Moraine C
Subjects: Abnormalities, Multiple genetics, Adult, Cataract genetics, Female, Humans, Intellectual Disability genetics, Kyphosis genetics, Male, Middle Aged, Pedigree, Pseudohypoparathyroidism genetics, Fibrous Dysplasia of Bone genetics, Fibrous Dysplasia, Polyostotic genetics, Osteoma genetics, Skin Neoplasms genetics
Abstract: Hereditary osteodystrophy of Albright's is a set of hereditary dystrophies associated or not with renal and bony resistance to the parathyroid hormone. Two observations of a true brotherhood are reported. These two patients had in common: short stature, obesity (especially facio-troncular), round face, flat and saddled nose, short neck, early cataract and mental deficiency. One of them showed fourth metacarpals. In these two cases there were cutaneous ossifications, markedly profuse on one of them than the other. These ossifications are a frequent manifestation of the osteodystrophy of Albright's. They appear as cutaneous nodules on any part of the body and are visible, palpable and present on X-ray examination. These ossifications share other phenotypic expressions of the disease and do not seem to be related to the resistance against parathyroid hormone.
Published: 1984

Author: Leroux-Robert J, Lièvre JA, Roulleau P, and Lacaille A
Subjects: Adolescent, Adult, Chromosome Aberrations, Chromosome Disorders, Female, Humans, Male, Maxillary Neoplasms diagnostic imaging, Maxillary Neoplasms surgery, Osteoma diagnostic imaging, Osteoma genetics, Osteoma surgery, Radiography, Bone Neoplasms genetics, Intestinal Polyps genetics, Neoplasms, Multiple Primary genetics, Osteomalacia genetics, Skin Neoplasms genetics
Published: 1973

Author: Sallet J, Helenon C, Becart C, and Parisot JP
Subjects: Abdominal Neoplasms genetics, Abdominal Neoplasms surgery, Adult, Chromosome Aberrations, Chromosome Disorders, Fibroma genetics, Humans, Intestinal Polyps diagnostic imaging, Intestinal Polyps genetics, Intestine, Small surgery, Male, Maxillary Neoplasms genetics, Mesenteric Arteries diagnostic imaging, Mesentery, Osteoma genetics, Peritoneal Neoplasms genetics, Radiography, Bone Neoplasms, Intestinal Neoplasms, Neoplasms, Multiple Primary, Skin Neoplasms
Published: 1969

Author: Schnyder UW
Subjects: Adenoma genetics, Carcinoma, Adenoid Cystic genetics, Genes, Dominant, Humans, Intestinal Polyps genetics, Keratoacanthoma genetics, Leiomyoma genetics, Lipomatosis genetics, Neoplasms, Multiple Primary genetics, Neurofibromatosis 1 genetics, Nevus genetics, Nevus, Pigmented genetics, Odontogenic Tumors genetics, Osteoma genetics, Papilloma genetics, Sebaceous Gland Neoplasms genetics, Skin Neoplasms genetics
Published: 1973

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