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509 results on '"Anodontia complications"'

501. The midline diastema.

Author

Baum AT

Subjects
Anodontia complications, Humans, Lingual Frenum pathology, Maxilla abnormalities, Maxilla embryology, Diastema etiology
Published
1966

503. Intermittent muscular weakness, extrasystoles, and multiple developmental anomalies. A new syndrome?

Author

Andersen ED, Krasilnikoff PA, and Overvad H

Subjects
Abnormalities, Multiple blood, Abnormalities, Multiple urine, Anodontia complications, Blepharoptosis complications, Cardiac Complexes, Premature drug therapy, Child, Cleft Palate complications, Cleidocranial Dysplasia complications, Craniofacial Dysostosis complications, Dwarfism complications, Ear, External abnormalities, Electrocardiography, Hand Deformities, Congenital, Heart Septal Defects, Ventricular complications, Humans, Male, Mandibulofacial Dysostosis complications, Phytotherapy, Plants, Medicinal, Procainamide therapeutic use, Propranolol therapeutic use, Rauwolfia therapeutic use, Abnormalities, Multiple complications, Cardiac Complexes, Premature complications, Muscular Atrophy complications
Published
1971
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505. Nosologic and genetic considerations in the aglossy-adactyly syndrome.

Author

Cohen MM Jr, Pantke H, and Siris E

Subjects
Abnormalities, Multiple classification, Abnormalities, Multiple genetics, Adolescent, Anodontia complications, Diagnosis, Differential, Ectromelia classification, Genes, Dominant, Genes, Recessive, Humans, Intellectual Disability complications, Male, Mandibulofacial Dysostosis classification, Syndrome, Arm abnormalities, Foot Deformities, Congenital, Mouth Abnormalities classification, Mouth Abnormalities complications, Mouth Abnormalities genetics, Tongue abnormalities
Abstract

A case of the aglossy-adactyly syndrome with a variety of associated anomalies and mental retardation suggests that the disorder may be a more complex dysmorphogenetic syndrome than is currently recognized. It is suggested that at least one and possibly two other conditions presently regarded as nosologically distinct from the aglossy-adactyly syndrome may, in fact, represent the same formal genesis syndrome. Because of the rarity of the condition, the failure to search for minor anomalies in first degree relatives and the lack of careful family histories in most cases, our present understanding of this syndrome is limited although etiologic heterogeneity seems likely.

Published
1971

507. [Zinsser-Cole-Engmann congenital dyskeratosis].

Author

Nazzaro P, Argentieri R, Bassetti F, Leonetti F, Topi G, and Valenzano L

Subjects
Alopecia complications, Anodontia complications, Atrophy complications, Female, Hand Dermatoses complications, Humans, Intellectual Disability complications, Leukoplakia, Oral complications, Male, Nails, Malformed complications, Scalp Dermatoses complications, Sex Factors, Splenomegaly complications, Syndrome, Tongue Diseases complications, Trachoma complications, Anemia, Aplastic complications, Keratosis complications, Mouth Diseases complications, Pigmentation Disorders complications
Published
1972

509. Micrognathia, hypodontia and syndactyly.

Author

Jorgenson RJ

Subjects
Child, Female, Heart Murmurs, Humans, Radiography, Skull diagnostic imaging, Tooth diagnostic imaging, Anodontia complications, Micrognathism complications, Syndactyly complications
Published
1971

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