Síndrome de Wiedemann y Beckwith: (macroglosia, onfalocele, macrosomía)

QR Code

Síndrome de Wiedemann y Beckwith: (macroglosia, onfalocele, macrosomía)

Saved in:

Bibliographic Details
Main Authors:	Mena R,María, Strickeler P,Alexis
Language:	Spanish / Castilian
Published:	Sociedad Chilena de Pediatría 1979
Subjects:	Síndrome de Wiedemann Beckwith macroglosia onfalocele macrosomía
Online Access:	http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0370-41061979000100009
Tags:	Add Tag No Tags, Be the first to tag this record!

Similar Items

Characteristics Associated with Tumor Development in Individuals Diagnosed with Beckwith–Wiedemann Spectrum: Novel Tumor-(epi)Genotype-Phenotype Associations in the BWSp Population
by: Kelly A. Duffy, et al.
Published: (2021)

Quantitative DNA Methylation Analysis and Epigenotype-Phenotype Correlations in Taiwanese Patients with Beckwith-Wiedemann Syndrome
by: Hsiang-Yu Lin, et al.
Published: (2021)

Beckwith–Wiedemann syndrome: Clinical, histopathological and molecular study of two Tunisian patients and review of literature
by: Hela Sassi, et al.
Published: (2021)

Síndrome de Beckwith-Wiedeman en Tres Hermanas
by: Almazán A,Carlos, et al.
Published: (1984)

Detection of hypermethylation at H19DMR at amniocentesis in a fetus with overgrowth, distended abdomen and Beckwith-Wiedemann syndrome
by: Chih-Ping Chen, et al.
Published: (2021)

Onfalocele
by: BOEHME VARGAS,CARLOS
Published: (1955)

Onfalocele, Divertículo de Meckel Permeable y Trisomia 13
by: Zúñiga R,Sergio, et al.
Published: (1986)

Amiloidosis AL y mieloma múltiple: Macroglosia como primera manifestación de una combinación infrecuente
by: García-Huidobro N,Francisco, et al.
Published: (2020)

Glosoplastía con Técnica de Harada en un Paciente con Síndrome de Down
by: Raposo,Araceli, et al.
Published: (2011)

Defectos de la pared abdominal: Estudio comparativo entre onfalocele y gastrosquisis
by: Nazer H,Julio, et al.
Published: (2013)

Ultrasonic predictors of macrosomia in gestational diabetes mellitus
by: Sergey N. Lysenko, et al.
Published: (2019)

Adrenocortical Tumors in Children With Constitutive Chromosome 11p15 Paternal Uniparental Disomy: Implications for Diagnosis and Treatment
by: Emilia Modolo Pinto, et al.
Published: (2021)

Cardiac pathologies in mouse loss of imprinting models are due to misexpression of H19 long noncoding RNA
by: Ki-Sun Park, et al.
Published: (2021)

The comparison of the effects of two Insulin therapy methods on fetal macrosomia due to maternal diabetes
by: M Faramarzi, et al.
Published: (1999)

Wiedemann–Steiner Syndrome with a Pathogenic Variant in <i>KMT2A</i> from Taiwan
by: Chung-Lin Lee, et al.
Published: (2021)

Prevalencia de defectos de la pared abdominal al nacer: Estudio ECLAMC
by: Nazer H,Julio, et al.
Published: (2006)

Three de novo variants in KMT2A (MLL) identified by whole exome sequencing in patients with Wiedemann–Steiner syndrome
by: Sukun Luo, et al.
Published: (2021)

Utilidad de la medición de fructosamina como indicador de control en pacientes con diabetes gestacional y pregestacional
by: Delgado M,Raúl, et al.
Published: (2011)

Divertículo de Meckel sintomático en pediatría
by: Urrutia Soto,Hugo, et al.
Published: (2021)

Análisis de la tasa de detección de fetos macrosómicos mediante ecografía
by: Teva G,María Jesús, et al.
Published: (2013)

MORBILIDAD FETAL ASOCIADA AL PARTO EN MACROSÓMICOS: ANÁLISIS DE 3981 NACIMIENTOS
by: Albornoz V.,Jaime, et al.
Published: (2005)

Perfil clínico de pacientes con diabetes gestacional e incidencia de complicaciones neonatales en un centro de referencia materno-fetal colombiano
by: Preciado,Lina Marcela Laverde, et al.
Published: (2020)

Niños macrosómicos y de peso normal de un consultorio de atención primaria. Comparación de características propias y maternas 1997-2000
by: López B,Ilse, et al.
Published: (2003)

Macroglosia y amiloidosis oculta
by: Moroni L,Ana María, et al.
Published: (2002)

The 6th International Symposium Diabetes and Pregnancy, 23-26 March 2011, Salzburg, Austria
by: Lyubov' Leonidovna Bolotskaya, et al.
Published: (2011)

Malformaciones cardiacas congénitas en el síndrome alcohólico fetal
by: Mena R,María, et al.
Published: (1986)

Birth weight and length in offsprings of mothers with gestational diabetes mellitus due to mutations in GCK gene
by: Natalia A. Zubkova, et al.
Published: (2018)

Síndrome cerebrohepatorrenal de Zellweger: una enfermedad peroxisomal
by: Rodillo B,Eliana, et al.
Published: (1996)

SINDROME DE EINSENMENGER Y EMBARAZO
by: Acuña S.,Margot, et al.
Published: (2002)

John Beckwith. In Search of Alberto Guerrero
by: Orrego-Salas,Juan
Published: (2008)

Tratamiento del síndrome nefrótico con corticoesteroides
by: DEL POZO P,HUMBERTO, et al.
Published: (1959)

CARACTERÍSTICAS DE NEONATOS MACROSÓMICOS Y DE SUS MADRES, DEL HOSPITAL HERMINDA MARTIN DE CHILLÁN
by: Mella V,Ivón, et al.
Published: (2006)

Assessment of the physical development and metabolic status of children born to women with gestational diabetes
by: A. S. Deynega (Masel), et al.
Published: (2021)

SINDROME ANTIFOSFOLIPIDOS Y EMBARAZO
by: Correa P.,Angel, et al.
Published: (2002)

Síndromes carenciales en la infancia
by: SCROGGIE,ARTURO
Published: (1941)

Síndrome de Jervell y Lange-Nielsen
by: Borkoski B,Silvia, et al.
Published: (2013)

Sindrome de Alpont
by: Rodríguez S,Eugenic, et al.
Published: (1984)

Síndrome Hemolítico Urémico
by: OCHOA,EDECIA, et al.
Published: (1973)

Síndrome Fetal Alcohólico: Estudio de 19 casos clínicos
by: Mena R,Maria, et al.
Published: (1980)

Síndrome de encefalopatía posterior reversible, eclampsia y síndrome de hellp
by: Álvarez-Pabón,Yelitza, et al.
Published: (2017)