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2. Juvenile Hyaline Fibromatosis is an Autosomal Recessive Genetic Disease. Four Cases Report

Author

Aparicio-Rodriguez J Manuel, Hurtado-Hernandez MdL, Barrientos-Perez Margarita, and Chatelain-Mercado Sergio

Subjects
Juvenile hyaline fibromatosis, Anal malformation, gingival hypertrophy, osteolitic lesions
Abstract

Juvenile hyaline fibromatosis (JHF) is considered a non frequent genetic, autosomic recessive; characterized by connective tissue disorder characterized by multiple subcutaneous nodules, gingival hypertrophy, osteolytic lesions, and joint deformities (contractures). As one of the main clinical symptoms, are multiple subcutaneous nodules, articular contractures, and gingival hypertrophy after 6 months of life. After one year old the subcutaneous nodules appears more frequently among teenagers a great variety of deformations are observed with movement limitations. 70 cases with JHC approximately are reported in the literature.

Published
2013

3. Aberraciones cromosómicas de pacientes pediátricos en 4617 estudios cromosómicos en un hospital de tercer nivel en un periodo de 19 años.

Author

Aparicio Rodríguez, Juan Manuel, Hurtado Hernández, María de Lourdes, Huitzil Muñoz, Enrique E., Marroquín García, Isabel, Rojas Rivera, Araceli, Barrientos Pérez, Margarita, Gómez Tello, Héctor, Rodríguez Peralta, Salvador, Zamudio Meneses, Rigoberto, Cuellar López, Fernando, Cubillo León, Marco Antonio, Sierra Pineda, Fátima, and Chatelain Mercado, Sergio

Subjects
CHROMOSOME abnormalities, KARYOTYPES, DNA, MEIOSIS, GENETIC mutation, ZYGOTES, DNA repair
Abstract

Copyright of Revista Oral is the property of Benemerita Universidad Autonoma de Puebla and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Published
2012

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