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Gurgel-Giannetti J ; Souza LS ; Messina de Pádua Andrade GF ; Derlene MF ; Meira ZMA ; Azevedo BVM ; Jr WC ; Diniz SSL ; Carvalhais MB ; Oliveira JRS ; Uliana L ; Bráulio R ; Costa PHN ; Filho GB ; Vainzof M | England | 21/09/2021Article
Biancalana V ; Rendu J ; Chaussenot A ; Mecili H ; Bieth E ; Fradin M ; Mercier S ; Michaud M ; Nougues MC ; Pasquier L ; Sacconi S ; Romero NB ; Marcorelles P ; Authier FJ ; Gelot Bernabe A ; Uro-Coste E ; Cances C ; Isidor B ; Magot A ; Minot-Myhie MC ; Pereon Y ; Perrier-Boeswillwald J ; Bretaudeau G ; Dondaine N ; Bouzenard A ; Pizzimenti M ; Eymard B ; Ferreiro A ; Laporte J ; Fauré J ; Bohm J | 17/09/2021Article
Suetterlin K ; Matthews E ; Sud R ; McCall S ; Fialho D ; Burge J ; Jayaseelan D ; Haworth A ; Sweeney MG ; Kullmann DM ; Schorge S ; Hanna MG ; Männikkö R | England | 16/09/2021Article
Alonso Perez J ; Gonzalez-Quereda L ; Bruno C ; Panicucci C ; Alavi A ; Nafissi S ; Nilipour Y ; Zanoteli E ; de Augusto Isihi LM ; Melegh B ; Hadzsiev K ; Muelas N ; Vilchez JJ ; Dourado ME ; Kadem N ; Kutluk G ; Umair M ; Younus M ; Pegorano E ; Bello L ; Crawford TO ; Suarez-Calvet X ; Topf A ; Guglieri M ; Marini-Bettolo C ; Gallano P ; Straub V ; Diaz-Manera J | England | 13/09/2021Article
Alghamdi F ; Al-Tawari A ; Alrohaif H ; Alshuaibi W ; Mansour H ; Aartsma Rus A ; Mégarbané A | 13/09/2021Article
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Initial Posting: June 8, 2000; Last Update: July 29, 2021.Article
Baumbach-Reardon L ; Hunter JM ; Ahearn ME ; Pfautsch M | 29/07/2021Initial Posting: October 30, 2008; Last Update: July 29, 2021.Article
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Weber F | 01/07/2021Initial Posting: July 18, 2003; Last Update: July 1, 2021. Clinical characteristics. Hyperkalemic periodic paralysis (hyperPP) is characterized by attacks of flaccid limb weakness (which may also include weakness of the muscles of the eyes[...]Article
Uchôa Cavalcanti EB ; Santos SCL ; Martins CES ; de Carvalho DR ; Rizzo IMPO ; Freitas MCDNB ; da Silva Freitas D ; de Souza FS ; Junior AM ; do Nascimento OJM | United States | 30/06/2021Article
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Malfatti E ; Catchpool T ; Nouioua S ; Sihem H ; Fournier E ; Carlier RY ; Cardone N ; Davis MR ; Laing NG ; Sternberg D ; Ravenscroft G | England | 23/06/2021Article
Bos JW ; Groen EJN ; Wadman RI ; Curial CAD ; Molleman NN ; Zegers M ; van Vught PWJ ; Snetselaar R ; Vijzelaar R ; van der Pol WL ; van den Berg LH | 22/06/2021Article
Botta A ; Visconti VV ; Fontana L ; Bisceglia P ; Bengala M ; Massa R ; Bagni I ; Cardani R ; Sangiuolo F ; Meola G ; Antonini G ; Petrucci A ; Pegoraro E ; D'Apice MR ; Novelli G | 21/06/2021Article
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Che WI ; Westerlind H ; Lundberg IE ; Hellgren K ; Kuja-Halkola R ; Holmqvist M | England | 15/06/2021Article
Creary LE ; Gangavarapu S ; Caillier SJ ; Cavalcante P ; Frangiamore R ; Lie BA ; Bengtsson M ; Harbo HF ; Brauner S ; Hollenbach JA ; Oksenberg JR ; Bernasconi P ; Maniaol AH ; Hammarström L ; Mantegazza R ; Fernández-Viña MA | 07/06/2021Article
Topf A ; Pyle A ; Griffin H ; Matalonga L ; Schon K ; Sickmann A ; Schara Schmidt U ; Hentschel A ; Chinnery PF ; Kolbel H ; Roos A ; Horvath R | England | 01/06/2021Article
Matalonga L ; Hernandez-Ferrer C ; Piscia D ; Schule R ; Synofzik M ; Topf A ; Vissers LELM ; de Voer R ; Tonda R ; Laurie S ; Fernandez-Callejo M ; Picó D ; Garcia-Linares C ; Papakonstantinou A ; Corvo A ; Joshi R ; Diez H ; Gut I ; Hoischen A ; Graessner H ; Beltran S | England | 01/06/2021Article
Aoki M ; Takahashi T | 27/05/2021Initial Posting: February 5, 2004; Last Update: May 27, 2021. Clinical characteristics. Dysferlinopathy includes a spectrum of muscle disease characterized by two major phenotypes: Miyoshi muscular dystrophy (MMD) and limb-girdle muscular [...]Article
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Takizawa H ; Mori Yoshimura M ; Minami N ; Murakami N ; Yatabe K ; Taira K ; Hashimoto Y ; Aoki Y ; Nishino I ; Takahashi Y | England | 27/04/2021Article
Initial Posting: June 11, 2015; Last Update: April 8, 2021 Clinical description. Riboflavin transporter deficiency (RTD), comprising RTD2 and RTD3 (caused by biallelic pathogenic variants in SLC52A2 and SLC52A3, respectively) is a rare neu[...]Article
Kutluk MG ; Kadem N ; Bektas O ; Randa NC ; Tuncer GO ; Albayrak P ; Eminoglu T ; Teber ST | 04/2021Article
Foley AR ; Mohassel P ; Donkervoort S ; Bolduc V ; Bonnemann CG | 11/03/2021Initial Posting: June 25, 2004; Last Update: March 11, 2021. Clinical characteristics. Collagen VI-related dystrophies (COL6-RDs) represent a continuum of overlapping clinical phenotypes with Bethlem muscular dystrophy at the milder end, U[...]Article
Azzedine H ; Salih MA | 11/03/2021Initial Posting: March 31, 2008; Last Update: March 11, 2021. Clinical characteristics. SH3TC2-related hereditary motor and sensory neuropathy (SH3TC2-HMSN) is a demyelinating neuropathy characterized by severe spine deformities (scoliosis[...]Article
Initial Posting: August 3, 2005; Last Update: February 25, 2021. Clinical characteristics. Myotonia congenita is characterized by muscle stiffness present from childhood; all striated muscle groups including the extrinsic eye muscles, faci[...]Article
Yalcintepe S ; Gurkan H ; Gungor Dogan I ; Demir S ; Ozemri Sag S ; Manav Kabayegit Z ; Atli EI ; Atli E ; Eker D ; Temel SG | Turkey | 22/02/2021Article
Lemmers RJLF ; van der Vliet PJ ; Blatnik A ; Balog J ; Zidar J ; Henderson D ; Goselink R ; Tapscott SJ ; Voermans NC ; Tawil R ; Padberg GWAM ; van Engelen BG ; van der Maarel SM | England | 12/01/2021Article
Kohlschmidt N ; Elbracht M ; Czech A ; Häusler M ; Phan V ; Topf A ; Huang KT ; Bartok A ; Eggermann K ; Zippel S ; Eggermann T ; Freier E ; Gross C ; Lochmuller H ; Horvath R ; Hajnoczky G ; Weis J ; Roos A | England | 11/01/2021Article
Velez-Bartolomei F ; Lee C ; Enns G | 07/01/2021Initial Posting: June 3, 2003; Last Update: January 7, 2021. Clinical characteristics. MERRF (myoclonic epilepsy with ragged red fibers) is a multisystem disorder characterized by myoclonus (often the first symptom) followed by generalized[...]Article
Prior TW ; Leach ME ; Finanger E | 3/12/2020Initial Posting: February 24, 2000; Last Revision: December 3, 2020. Clinical characteristics. Spinal muscular atrophy (SMA) is characterized by muscle weakness and atrophy resulting from progressive degeneration and irreversible loss of t[...]Article
Trollet C ; Boulinguiez A ; Roth F ; Stojkovic T ; Butler Browne G ; Evangelista T ; Lacau St Guily J ; Richard P | 22/10/2020Initial Posting: March 8, 2001; Last Update: October 22, 2020. Clinical characteristics. Oculopharyngeal muscular dystrophy (OPMD) is characterized by ptosis and dysphagia due to selective involvement of the muscles of the eyelids and phar[...]Article
McCray BA ; Schindler A ; Hoover-Fong JE ; Sumner CJ | 17/09/2020Initial Posting: May 15, 2014; Last Update: September 17, 2020. Clinical characteristics. The autosomal dominant TRPV4 disorders (previously considered to be clinically distinct phenotypes before their molecular basis was discovered) are n[...]Article
Initial Posting: April 2, 2009; Last Update: September 17, 2020. Clinical characteristics. Most individuals with classic GBE1 adult polyglucosan body disease (GBE1-APBD) present after age 40 years with unexplained progressive neurogenic bl[...]Article
Oliveira J ; Parente Freixo J ; Santos M ; Coelho T | 17/09/2020Initial Posting: June 7, 2012; Last Update: September 17, 2020. Clinical characteristics. The clinical manifestations of LAMA2 muscular dystrophy (LAMA2-MD) comprise a continuous spectrum ranging from severe congenital muscular dystrophy t[...]Article
Chrestian N | 27/08/2020Initial Posting: September 28, 1998; Last Update: August 27, 2020. Clinical characteristics. Hereditary neuropathy with liability to pressure palsies (HNPP) is characterized by recurrent acute sensory and motor neuropathy in a single or mu[...]Article
Ferreira C ; Pierre G ; Thompson R ; Vernon H | 09/07/2020nitial Posting: October 9, 2014; Last Update: July 9, 2020. Clinical characteristics. Barth syndrome is characterized in affected males by cardiomyopathy, neutropenia, skeletal myopathy, prepubertal growth delay, and distinctive facial ges[...]Article
Deng J ; Yu J ; Li P ; Luan X ; Cao L ; Zhao J ; Yu M ; Zhang W ; Lv H ; Xie Z ; Meng L ; Zheng Y ; Zhao Y ; Gang Q ; Wang Q ; Liu J ; Zhu M ; Guo X ; Su Y ; Liang Y ; Liang F ; Hayashi T ; Maeda MH ; Sato T ; Ura S ; Oya Y ; Ogasawara M ; Iida A ; Nishino I ; Zhou C ; Yan C ; Yuan Y ; Hong D ; Wang Z | United States | 07/2020Article
Prasun P | 18/06/2020Clinical characteristics. Multiple acyl-CoA dehydrogenase deficiency (MADD) represents a clinical spectrum in which presentations can be divided into type I (neonatal onset with congenital anomalies), type II (neonatal onset without congenita[...]Article
Echaniz-Laguna A ; Biancalana V ; Nadaj-Pakleza A ; Fournier E ; Matthews E ; Hanna MG ; MÀnnikkà R | England | 06/2020Article
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Benquey T ; Fockens E ; Kouton L ; Delmont E ; Martini N ; Levy N ; Attarian S ; Bonello-Palot N | Netherlands | 06/2020Article
Gharesouran J ; Jalaiei A ; Hosseinzadeh A ; Ghafouri-Fard S ; Mokhtari Z ; Ghahremanzadeh K ; Rezazadeh N ; Shiva S ; Sadeghvand S ; Taheri M ; Rezazadeh M | United States | 06/2020Article
Hamanaka K ; Sikrova D ; Mitsuhashi S ; Masuda H ; Sekiguchi Y ; Sugiyama A ; Shibuya K ; Lemmers RJLF ; Goossens R ; Ogawa M ; Nagao K ; Obuse C ; Noguchi S ; Hayashi YK ; Kuwabara S ; Balog J ; Nishino I ; van der Maarel SM | United States | 06/2020Article
Zuchner S | 14/05/2020Initial Posting: February 18, 2005; Last Update: May 14, 2020. Clinical characteristics. MFN2 hereditary motor and sensory neuropathy (MFN2-HMSN) is a classic axonal peripheral sensorimotor neuropathy, inherited in either an autosomal domi[...]Article
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Rodolico C ; Politano L ; Portaro S ; Murru S ; Boccone L ; Sera F ; Passamano L ; Brizzi T ; Tupler R | England | 05/2020Article
Gonzalez-Quereda L ; Rodriguez MJ ; Diaz-Manera J ; Alonso Perez J ; Gallardo E ; Nascimento A ; Ortez C ; Benito DN ; Olive M ; Gonzalez Mera L ; Munain AL ; Zulaica M ; Poza JJ ; Jerico I ; Torne L ; Riera P ; Milisenda J ; Sanchez A ; Garrabou G ; Llano I ; Madruga-Garrido M ; Gallano P | Switzerland | 05/2020Article
Lorenzoni PJ ; Kay CSK ; Arndt RC ; Hrysay NMC ; Ducci RD ; Fustes OHJ ; Topf A ; Lochmuller H ; Werneck LC ; Scola RH | Scotland | 05/2020Article
Zamani G ; Hosseini Bereshneh A ; Azizi Malamiri R ; Bagheri S ; Moradi K ; Ashrafi MR ; Tavasoli AR ; Mohammadi M ; Badv RS ; Ghahvechi Akbari M ; Heidari M | United States | 05/2020Article
Morizumi T ; Ueno A ; Takasone K ; Ozawa K ; Yoshinaga T ; Nakamura K ; Sekijima Y | Netherlands | 05/2020Article
Al-Muhaizea MA ; AlQuait L ; AlRasheed A ; AlHarbi S ; Albader AA ; AlMass R ; Albakheet A ; Alhumaidan A ; AlRasheed MM ; Colak D ; Kaya N | England | 05/2020Article
Carrillo N ; Malicdan MC ; Huizing M | 09/04/2020Initial Posting: March 26, 2004; Last Update: April 9, 2020. Clinical characteristics. GNE myopathy is a slowly progressive muscle disease that typically presents between age 20 and 40 years with bilateral foot drop caused by anterior tibial[...]Article
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Ohkawara B ; Shen X ; Selcen D ; Nazim M ; Bril V ; Tarnopolsky MA ; Brady L ; Fukami S ; Amato AA ; Yis U ; Ohno K ; Engel AG | United States | 04/2020Article
Geroldi A ; Prada V ; Veneri F ; Trevisan L ; Origone P ; Grandis M ; Schenone A ; Gemelli C ; Lanteri P ; Fossa P ; Mandich P ; Bellone E | United States | 04/2020Article
Abdel Aleem A ; Elsaid MF ; Chalhoub N ; Chakroun A ; Mohamed KAS ; AlShami R ; Kuzu O ; Mohamed RB ; Ibrahim K ; AlMudheki N ; Osman O ; Ross ME ; ELalamy O | England | 04/2020Article
Keller N ; Mendoza-Ferreira N ; Maroofian R ; Chelban V ; Khalil Y ; Mills PB ; Boostani R ; Torbati PN ; Karimiani EG ; Thiele H ; Houlden H ; Wirth B ; Karakaya M | England | 04/2020Article
Lee CY, Auteur ; Petkova M ; Morales-Gonzalez S ; Gimber N ; Schmoranzer J ; Meisel A ; Bohmerle W ; Stenzel W ; Schuelke M ; Schwarz JM | England | 04/2020Article
Vanherpe P ; Fieuws S ; D'Hondt A ; Bleyenheuft C ; Demaerel P ; De Bleecker J ; van den Bergh P ; Baets J ; Remiche G ; Verhoeven K ; Delstanche S ; Toussaint M ; Buyse B ; Van Damme P ; Depuydt CE ; Claeys KG | 04/2020Article
Schoser B | 19/03/2020Initial Posting: September 21, 2006; Last Update: March 19, 2020. Clinical characteristics. Myotonic dystrophy type 2 (DM2) is characterized by myotonia and muscle dysfunction (proximal and axial weakness, myalgia, and stiffness), and less[...]Article
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El Kadiri Y ; Selouani Y ; Ratbi I ; Lyahyai J ; Zrhidri A ; Sahli M ; Ouhenach M ; Jaouad IC ; Sefiani A ; Sbiti A | Netherlands | 03/2020Article
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Joosten IBT ; Hellebrekers DMEI ; de Greef BTA ; Smeets HJM ; De Die-Smulders CEM ; Faber CG ; Gerrits MM | England | 03/2020Article
Neri M ; Rossi R ; Trabanelli C ; Mauro A ; Selvatici R ; Falzarano MS ; Spedicato N ; Margutti A ; Rimessi P ; Fortunato F ; Fabris M ; Gualandi F ; Comi G ; Tedeschi S ; Seia M ; Fiorillo C ; Traverso M ; Bruno C ; Giardina E ; Piemontese MR ; Merla G ; Cau M ; Marica M ; Scuderi C ; Borgione E ; Tessa A ; Astrea G ; Santorelli FM ; Merlini L ; Mora M ; Bernasconi P ; Gibertini S ; Sansone V ; Mongini T ; Berardinelli A ; Pini A ; Liguori R ; Filosto M ; Messina S ; Vita G ; Toscano A ; Vita G ; Pane M ; Servidei S ; Pegoraro E ; Bello L ; Travaglini L ; Bertini E ; D'Amico A ; Ergoli M ; Politano L ; Torella A ; Nigro V ; Mercuri E ; Ferlini A | 03/2020Article
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Abrams CK | 20/02/2020Initial Posting: June 18, 1998; Last Update: February 20, 2020. Clinical characteristics. GJB1 disorders are typically characterized by peripheral motor and sensory neuropathy with or without fixed CNS abnormalities and/or acute, self-limite[...]Article
Preston MK ; Tawil R ; Wang LH | 06/02/2020Initial Posting: March 8, 1999; Last Update: February 6, 2020. Clinical characteristics. Facioscapulohumeral muscular dystrophy (FSHD) typically presents with weakness of the facial muscles, the stabilizers of the scapula, or the dorsiflexor[...]Article
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Rosenberg H ; Sambuughin N ; Riazi S ; Dirksen R | 16/01/2020Initial Posting: December 19, 2003; Last Update: January 16, 2020. Clinical characteristics. Malignant hyperthermia susceptibility (MHS) is a pharmacogenetic disorder of skeletal muscle calcium regulation associated with uncontrolled skeleta[...]Article
Initial Posting: February 17, 2005; Last Update: January 2, 2020. Clinical characteristics. Udd distal myopathy – tibial muscular dystrophy (UDM-TMD) is characterized by weakness of ankle dorsiflexion and inability to walk on the heels aft[...]Article
Bevilacqua JA ; Guecaimburu Ehuletche MDR ; Perna A ; Dubrovsky A ; Franca MC Jr ; Vargas S ; Hegde M ; Claeys KG ; Straub V ; Daba N ; Faria R ; Periquet M ; Sparks S ; Thibault N ; Araujo R | England | 01/2020Article
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Akesson LS ; Savarirayan R | 2020Clinical characteristics. Fibrodysplasia ossificans progressiva (FOP) is characterized by congenital bilateral hallux valgus malformations and early-onset heterotopic ossification, which may be spontaneous or precipitated by trauma including [...]Article
Landires I ; Nunez-Samudio V ; Fernandez J ; Sarria C ; Villareal V ; Cordoba F ; Apraez-Ippolito G ; Martinez S ; Vidal OM ; Velez JI ; Arcos-Holzinger M ; Landires S ; Arcos-Burgos M | Switzerland | 01/2020Article
Topf A ; Johnson K ; Bates A ; Phillips L ; Chao KR ; England EM ; Laricchia KM ; Mullen T ; Valkanas E ; Xu L ; Bertoli M ; Blain A ; Casasus AB ; Duff J ; Mroczek M ; Specht S ; Lek M ; Ensini M ; Macarthur DG ; Straub V | United States | 2020Article
Forrester N ; Rattihalli R ; Horvath R ; Maggi L ; Manzur A ; Fuller G ; Gutowski N ; Rankin J ; Dick D ; Buxton C ; Greenslade M ; Majumdar A | Netherlands | 2020Article
Muller Felber W ; Vill K ; Schwartz O ; Glaser D ; Nennstiel U ; Wirth B ; Burggraf S ; Roschinger W ; Becker M ; Durner J ; Eggermann K ; Muller C ; Hannibal I ; Olgemoller B ; Schara U ; Blaschek A ; Kolbel H | Netherlands | 2020Article
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Gentile L ; Russo M ; Fabrizi GM ; Taioli F ; Ferrarini M ; Testi S ; Alfonzo A ; Aguennouz M ; Toscano A ; Vita G ; Mazzeo A | Italy | 01/2020Article
Cortese A ; Wilcox JE ; Polke JM ; Poh R ; Skorupinska M ; Rossor AM ; Laura M ; Tomaselli PJ ; Houlden H ; Shy ME ; Reilly MM | United States | 01/2020