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conseil génétiqueSynonyme(s)genetic counselling ;génétique conseil ;consultation génétique genetic counseling |
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Azad AK ; Huang CK ; Jin H ; Zou H ; Yanakakis L ; Du J ; Fiddler M ; Naeem R ; Goldstein Y | England | 12/2019Article
Greenbaum L ; Barel O ; Nikitin V ; Hersalis-Eldar A ; Kol N ; Reznik-Wolf H ; Dominissini D ; Pras E ; Dori A | United States | 12/2019Article
De Ridder W ; Azmi A ; Clemen CS ; Eichinger L ; Hofmann A ; Schröder R ; Johnson K ; Topf A ; Straub V ; De Jonghe P ; Maudsley S ; De Bleecker JL ; Baets J | United States | 12/2019Article
Labrador E ; Weinstein DA | 27/11/2019Initial Posting: April 23, 2009; Last Update: November 27, 2019. Clinical characteristics. Glycogen storage disease type VI (GSD VI) is a disorder of glycogenolysis caused by deficiency of hepatic glycogen phosphorylase. This critical enzy[...]Article
Urtizberea JA ; Alrohaif H ; Gouda SA ; Bastaki L | AFM-TELETHON | Les cahiers de myologie | 11/2019Les myopathies congénitales constituent un ensemble hétérogène de maladies neuromusculaires aussi bien sur le plan clinique que génétique. Le séquençage à haut débit, ciblé ou non, couplé à l’analyse de la biopsie musculaire, facilite grandement[...]Article
Mojbafan M, Auteur ; Tina S ; Zafarghandi Motlagh F ; Surguchov A ; Nilipour Y ; Zeinali S | United States | 11/2019Article
Wang H, Auteur ; Kacar Bayram A ; Sprute R ; Ozdemir O ; Cooper E ; Pergande M ; Efthymiou S ; Nedic I ; Mazaheri N ; Stumpfe K ; Azizi Malamiri R ; Shariati G ; Zeighami J ; Bayram N ; Naghibzadeh SK ; Tajik M ; Yasar M ; Sami Guven A ; Bibi F ; Sultan T ; Salpietro V ; Houlden H ; Per H ; Galehdari H ; Shalbafan B ; Jamshidi Y ; Cirak S | Switzerland | 10/2019Article
von der Hagen M, Auteur ; Becker LL ; Wienker TF ; Smitka M ; Musante L ; Ropers HH ; Huebner A ; Hu H ; Kaindl AM | Germany | 10/2019Publication AFM
Myoinfo, Auteur ; Duguet C, Validateur ; Dupitier E, Validateur ; Eymard N, Validateur ; Lagrue E, Validateur ; Reveillere C, Validateur ; Urtizberea JA | AFM-TELETHON | Savoir & Comprendre | 10/2019L’amyotrophie spinale proximale liée au gène SMN1 est une maladie rare qui se manifeste par une faiblesse musculaire d’importance variable exceptionnellement présente dès la naissance ou apparaissant par la suite, dans l’enfance, à l’adolescence[...]Article
Kimonis V | 12/09/2019Initial Posting: May 25, 2007; Last Update: September 12, 2019. Clinical characteristics. Inclusion body myopathy associated with Paget disease of bone (PDB) and/or frontotemporal dementia (IBMPFD) is characterized by adult-onset proximal [...]Article
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Penttila S ; Vihola A ; Palmio J ; Udd B | 22/08/2019Initial Posting: November 29, 2012; Last Update: August 22, 2019. Clinical characteristics. The spectrum of ANO5 muscle disease is a continuum that ranges from asymptomatic hyperCKemia and exercise-induced myalgia to proximal and/or distal m[...]Article
Bonne G ; Leturcq F ; Ben Yaou R | 15/08/2019Initial Posting: September 29, 2004; Last Update: August 15, 2019. Clinical characteristics. Emery-Dreifuss muscular dystrophy (EDMD) is characterized by the clinical triad of: joint contractures that begin in early childhood; slowly progr[...]Article
Magoulas PL ; El-Hattab AW | 01/08/2019Initial Posting: January 3, 2013; Last Update: August 1, 2019. Clinical characteristics. The clinical manifestations of glycogen storage disease type IV (GSD IV) discussed in this entry span a continuum of different subtypes with variable ag[...]Article
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Saito K | 03/07/2019Initial Posting: January 26, 2006; Last Update: July 3, 2019. Clinical characteristics. Fukuyama congenital muscular dystrophy (FCMD) is characterized by hypotonia, symmetric generalized muscle weakness, and CNS migration disturbances that[...]Article
Initial Posting: April 19, 2006; Last Update: June 20, 2019. Clinical characteristics. Glycogen storage disease type V (GSDV, McArdle disease) is a metabolic myopathy characterized by exercise intolerance manifested by rapid fatigue, myalgia[...]Article
Initial Posting: June 20, 2019. Clinical characteristics. STAC3 disorder is characterized by congenital myopathy, musculoskeletal involvement of the trunk and extremities, feeding difficulties, and delayed motor milestones. Most affected ind[...]Article
Initial Posting: August 5, 2008; Last Update: June 6, 2019. The purpose of this overview is to increase clinician awareness of the genetic basis of hypertrophic cardiomyopathy (HCM) and the benefits of early diagnosis and management to indivi[...]Reco PNDS
Ce document est la traduction de la publication "Consensus-based Care Recommendations for Adults with Myotonic Dystrophy Type 1" édité par la « Myotonic Dystrophy Foundation ». SOMMAIRE Symptômes mettant la vie en danger - Chirurgie, anesthés[...]Article
Hackman P ; Savarese M ; Carmignac V ; Udd B ; Salih MA | 11/04/2019Initial Posting: January 12, 2012; Last Update: April 11, 2019. Clinical characteristics. Salih myopathy is characterized by muscle weakness (manifest during the neonatal period or in early infancy) and delayed motor development; children ac[...]