Literature DB >> 6512833

Chronic proximal spinal muscular atrophy of childhood and adolescence: sex influence.

I Hausmanowa-Petrusewicz, J Zaremba, J Borkowska, W Szirkowiec.   

Abstract

Segregation analysis was performed on 354 cases of chronic proximal spinal muscular atrophy of childhood and adolescence (CPSMA) in the total series and in a number of subgroups formed according to the age at onset and sex. The analysis provided evidence of sex influence in the series studied, particularly in a subgroup of the milder form of the disease with onset between the 37th month and 18th year of life. In the latter subgroup, females were affected much less frequently. This was particularly striking after age at onset of 8 years, and only exceptionally were females affected after the age of 13 years. These facts point to incomplete penetrance of the gene.

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Year:  1984        PMID: 6512833      PMCID: PMC1049345          DOI: 10.1136/jmg.21.6.447

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  22 in total

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Journal:  Acta Neurol (Napoli)       Date:  1969 May-Jun

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Authors:  T Namba; D C Aberfeld; D Grob
Journal:  J Neurol Sci       Date:  1970-11       Impact factor: 3.181

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  7 in total

1.  Population data on acute infantile and chronic childhood spinal muscular atrophy in Warsaw.

Authors:  A W Spiegler; I Hausmanowa-Pertrusewicz; J Borkowska; A Kłopocka
Journal:  Hum Genet       Date:  1990-07       Impact factor: 4.132

2.  Gender Effects on the Clinical Phenotype in Japanese Patients with Spinal Muscular Atrophy.

Authors:  Mawaddah Ar Rochmah; Ai Shima; Nur Imma Fatimah Harahap; Emma Tabe Eko Niba; Naoya Morisada; Shinichiro Yanagisawa; Toshio Saito; Kaori Kaneko; Kayoko Saito; Ichiro Morioka; Kazumoto Iijima; Poh San Lai; Yoshihiro Bouike; Hisahide Nishio; Masakazu Shinohara
Journal:  Kobe J Med Sci       Date:  2017-10-16

3.  Chronic proximal spinal muscular atrophy of childhood and adolescence: problems of classification and genetic counselling.

Authors:  I Hausmanowa-Petrusewicz; J Zaremba; J Borkowska
Journal:  J Med Genet       Date:  1985-10       Impact factor: 6.318

4.  Mutation update of spinal muscular atrophy in Spain: molecular characterization of 745 unrelated patients and identification of four novel mutations in the SMN1 gene.

Authors:  Laura Alías; Sara Bernal; Pablo Fuentes-Prior; María Jesus Barceló; Eva Also; Rebeca Martínez-Hernández; Francisco J Rodríguez-Alvarez; Yolanda Martín; Elena Aller; Elena Grau; Ana Peciña; Guillermo Antiñolo; Enrique Galán; Alberto L Rosa; Miguel Fernández-Burriel; Salud Borrego; José M Millán; Concepción Hernández-Chico; Montserrat Baiget; Eduardo F Tizzano
Journal:  Hum Genet       Date:  2008-12-03       Impact factor: 4.132

5.  Complex repetitive arrangements of gene sequence in the candidate region of the spinal muscular atrophy gene in 5q13.

Authors:  A M Theodosiou; K E Morrison; A M Nesbit; R J Daniels; L Campbell; M J Francis; Z Christodoulou; K E Davies
Journal:  Am J Hum Genet       Date:  1994-12       Impact factor: 11.025

6.  Observation of the natural course of type 3 spinal muscular atrophy: data from the polish registry of spinal muscular atrophy.

Authors:  Anna Lusakowska; Maria Jedrzejowska; Anna Kaminska; Katarzyna Janiszewska; Przemysław Grochowski; Janusz Zimowski; Janusz Sierdzinski; Anna Kostera-Pruszczyk
Journal:  Orphanet J Rare Dis       Date:  2021-03-24       Impact factor: 4.123

7.  The Occurrence of 275 Rare Diseases and 47 Rare Disease Groups in Italy. Results from the National Registry of Rare Diseases.

Authors:  Domenica Taruscio; Luciano Vittozzi; Adele Rocchetti; Paola Torreri; Luca Ferrari
Journal:  Int J Environ Res Public Health       Date:  2018-07-12       Impact factor: 3.390

  7 in total

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