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Documents disponibles dans cette catégorie (2176)
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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[...]