glycogen and Hernia--Inguinal

glycogen has been researched along with Hernia--Inguinal* in 2 studies

Other Studies

2 other study(ies) available for glycogen and Hernia--Inguinal

Article	Year
Arthrogryposis multiplex with deafness, inguinal hernias, and early death: a family report of a probably autosomal recessive trait. American journal of medical genetics. Part A, 2005, Aug-30, Volume: 137, Issue:2 We report on three male newborn infants of a highly inbred Lebanese family presenting with a characteristic phenotype: arthrogryposis multiplex, deafness, large inguinal hernia, hiccup-like diaphragmatic contractions, and inability to suck, requiring nasogastric gavage feeding. All three boys died from respiratory failure during the first 3 months of life. Intra vitam or post mortem examinations revealed myopathic changes and elevated glycogen content of muscle tissue. This new syndrome is probably transmitted in an autosomal recessive mode, although X-linked inheritance cannot be excluded. Topics: 1,4-alpha-Glucan Branching Enzyme; Abnormalities, Multiple; Arthrogryposis; Consanguinity; Deafness; Family Health; Fatal Outcome; Female; Genes, Recessive; Glycogen; Hernia, Inguinal; Humans; Infant; Infant, Newborn; Male; Pedigree; Phosphorylase a; Polymorphism, Single Nucleotide	2005
Ultrastructural aspects of Sertoli cells in infancy. Bollettino della Societa italiana di biologia sperimentale, 1979, Feb-28, Volume: 55, Issue:4 In the present study some aspects of Sertoli cells of testicular-biopsy specimens of children from 0 to 8 years old are examined. We can distinguish two main morphological situations. In the first one, Sertoli cells with monomorphic aspect can be seen; in the second can be shown Sertoli cells with various aspects. In this polimorphic situation we can distinguish three Sertoli cell types differing in cellular shape, cytoplasme electron-density and amount of RER and Golgi complex. Topics: Biopsy; Child; Child, Preschool; Glycogen; Hernia, Inguinal; Humans; Infant; Male; Microscopy, Electron; Sertoli Cells; Testis	1979

Article

Year

Arthrogryposis multiplex with deafness, inguinal hernias, and early death: a family report of a probably autosomal recessive trait.

American journal of medical genetics. Part A, 2005, Aug-30, Volume: 137, Issue:2

We report on three male newborn infants of a highly inbred Lebanese family presenting with a characteristic phenotype: arthrogryposis multiplex, deafness, large inguinal hernia, hiccup-like diaphragmatic contractions, and inability to suck, requiring nasogastric gavage feeding. All three boys died from respiratory failure during the first 3 months of life. Intra vitam or post mortem examinations revealed myopathic changes and elevated glycogen content of muscle tissue. This new syndrome is probably transmitted in an autosomal recessive mode, although X-linked inheritance cannot be excluded.

Topics: 1,4-alpha-Glucan Branching Enzyme; Abnormalities, Multiple; Arthrogryposis; Consanguinity; Deafness; Family Health; Fatal Outcome; Female; Genes, Recessive; Glycogen; Hernia, Inguinal; Humans; Infant; Infant, Newborn; Male; Pedigree; Phosphorylase a; Polymorphism, Single Nucleotide

2005

Ultrastructural aspects of Sertoli cells in infancy.

Bollettino della Societa italiana di biologia sperimentale, 1979, Feb-28, Volume: 55, Issue:4

In the present study some aspects of Sertoli cells of testicular-biopsy specimens of children from 0 to 8 years old are examined. We can distinguish two main morphological situations. In the first one, Sertoli cells with monomorphic aspect can be seen; in the second can be shown Sertoli cells with various aspects. In this polimorphic situation we can distinguish three Sertoli cell types differing in cellular shape, cytoplasme electron-density and amount of RER and Golgi complex.

Topics: Biopsy; Child; Child, Preschool; Glycogen; Hernia, Inguinal; Humans; Infant; Male; Microscopy, Electron; Sertoli Cells; Testis

1979