Moderately progressive Ullrich congenital muscular dystrophy. 2012

Gerson Carakushansky, and Marcia Gonçalves Ribeiro, and Evelyn Kahn
Universidade Federal do Rio de Janeiro (UFRJ), Rio de Janeiro, RJ, Brazil. clinicagenetica@gmail.com

OBJECTIVE To describe genetic and clinical features of Ullrich congenital muscular dystrophy (UCMD), and to report the case of a patient diagnosed with UCMD after an exhaustive investigation, which included collagen VI immunohistochemical and genomic analyses. METHODS This study was based on clinical, immunohistochemical assessment of muscle tissue and genomic analysis of dermal fibroblasts of a 7 1/2-year old boy and of the DNA of his parents. Clinical aspects and differential diagnosis with other disorders are discussed. CONCLUSIONS A better knowledge of congenital muscular dystrophies will improve the number of correct diagnoses and open new horizons for the treatment of such diseases. Genetic evaluation of UCMD patients has relevant implications for prognosis and genetic counseling of the family. The dissemination of this disorder in the pediatric community is advisable, because of the early onset of clinical manifestations and the fact that it is frequently misdiagnosed or not diagnosed at all.

UI MeSH Term Description Entries
D007150 Immunohistochemistry Histochemical localization of immunoreactive substances using labeled antibodies as reagents. Immunocytochemistry,Immunogold Techniques,Immunogold-Silver Techniques,Immunohistocytochemistry,Immunolabeling Techniques,Immunogold Technics,Immunogold-Silver Technics,Immunolabeling Technics,Immunogold Silver Technics,Immunogold Silver Techniques,Immunogold Technic,Immunogold Technique,Immunogold-Silver Technic,Immunogold-Silver Technique,Immunolabeling Technic,Immunolabeling Technique,Technic, Immunogold,Technic, Immunogold-Silver,Technic, Immunolabeling,Technics, Immunogold,Technics, Immunogold-Silver,Technics, Immunolabeling,Technique, Immunogold,Technique, Immunogold-Silver,Technique, Immunolabeling,Techniques, Immunogold,Techniques, Immunogold-Silver,Techniques, Immunolabeling
D008297 Male Males
D009136 Muscular Dystrophies A heterogeneous group of inherited MYOPATHIES, characterized by wasting and weakness of the SKELETAL MUSCLE. They are categorized by the sites of MUSCLE WEAKNESS; AGE OF ONSET; and INHERITANCE PATTERNS. Muscular Dystrophy,Myodystrophica,Myodystrophy,Dystrophies, Muscular,Dystrophy, Muscular,Myodystrophicas,Myodystrophies
D009154 Mutation Any detectable and heritable change in the genetic material that causes a change in the GENOTYPE and which is transmitted to daughter cells and to succeeding generations. Mutations
D010290 Parents Persons functioning as natural, adoptive, or substitute parents. The heading includes the concept of parenthood as well as preparation for becoming a parent. Step-Parents,Parental Age,Parenthood Status,Stepparent,Age, Parental,Ages, Parental,Parent,Parental Ages,Status, Parenthood,Step Parents,Step-Parent,Stepparents
D002648 Child A person 6 to 12 years of age. An individual 2 to 5 years old is CHILD, PRESCHOOL. Children
D003937 Diagnosis, Differential Determination of which one of two or more diseases or conditions a patient is suffering from by systematically comparing and contrasting results of diagnostic measures. Diagnoses, Differential,Differential Diagnoses,Differential Diagnosis
D004252 DNA Mutational Analysis Biochemical identification of mutational changes in a nucleotide sequence. Mutational Analysis, DNA,Analysis, DNA Mutational,Analyses, DNA Mutational,DNA Mutational Analyses,Mutational Analyses, DNA
D005347 Fibroblasts Connective tissue cells which secrete an extracellular matrix rich in collagen and other macromolecules. Fibroblast
D005817 Genetic Counseling An educational process that provides information and advice to individuals or families about a genetic condition that may affect them. The purpose is to help individuals make informed decisions about marriage, reproduction, and other health management issues based on information about the genetic disease, the available diagnostic tests, and management programs. Psychosocial support is usually offered. Counseling, Genetic,Genetic Counseling, Prenatal,Prenatal Genetic Counseling

Related Publications

Gerson Carakushansky, and Marcia Gonçalves Ribeiro, and Evelyn Kahn
September 2013, Journal of neurology, neurosurgery, and psychiatry,
Gerson Carakushansky, and Marcia Gonçalves Ribeiro, and Evelyn Kahn
November 2005, Rinsho shinkeigaku = Clinical neurology,
Gerson Carakushansky, and Marcia Gonçalves Ribeiro, and Evelyn Kahn
January 1991, Neurologia (Barcelona, Spain),
Gerson Carakushansky, and Marcia Gonçalves Ribeiro, and Evelyn Kahn
May 2021, Anesthesiology,
Gerson Carakushansky, and Marcia Gonçalves Ribeiro, and Evelyn Kahn
July 2009, Neurology,
Gerson Carakushansky, and Marcia Gonçalves Ribeiro, and Evelyn Kahn
December 2008, Neuromuscular disorders : NMD,
Gerson Carakushansky, and Marcia Gonçalves Ribeiro, and Evelyn Kahn
January 1954, Zeitschrift fur Kinderheilkunde,
Gerson Carakushansky, and Marcia Gonçalves Ribeiro, and Evelyn Kahn
January 2016, Frontiers in aging neuroscience,
Gerson Carakushansky, and Marcia Gonçalves Ribeiro, and Evelyn Kahn
January 2013, Iranian journal of child neurology,
Gerson Carakushansky, and Marcia Gonçalves Ribeiro, and Evelyn Kahn
August 2013, Neurology,
Copied contents to your clipboard!