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PATHOLOGIC FINDINGS in the WOLF-HIRSCHHORN (4P-) SYNDROME

Gonzalez, C. H.
Capelozzi, V. L.
Wajntal, A.

Publication date

January 1981

DOI

10.1002/ajmg.1320090303

Publisher

Wiley

ISSN

0148-7299

Journal

American Journal of Medical Genetics

Citation count (estimate)

6

Abstract

UNIV São Paulo,FAC MED,DEPT PATHOL,São Paulo,BRAZILUNIV São Paulo,FAC MED,MED GENET LAB,São Paulo,BRAZILWeb of Scienc

Extracted data

Related items

Wolf-Hirschhorn (4p-) syndrome: Prenatal diagnosis, molecular cytogenetic characterization and association with a 1.2-Mb microduplication at 8p22-p21.3 and a 1.1-Mb microduplication at 10p15.3 in a fetus with an apparently pure 4p deletion

Chen, Chih-Ping
Su, Yi-Ning
Chen, Yi-Yung
Su, Jun-Wei
Chern, Schu-Rern
Chen, Yu-Ting
Chen, Wen-Lin
Chen, Li-Feng
Wang, Wayseen

December 2011

AbstractObjectiveTo present prenatal diagnosis and molecular cytogenetic characterization of Wolf-Hi...

Wolf-Hirschhorn syndrome revealed by status epilepticus: A case report

IMANE FILALI
HABIBA EL YATIM
ABDELILAH RADI
RACHID ABILKACEM
AOMAR AGADR

January 2023

A Wolf-Hirschhorn syndrome is a rare chromosomal anomaly, which results from a deletion of the dista...

Syndrome de Wolf Hirschhorn à propos d’un cas

RAQUI, Aniss

January 2012

le syndrome de Wolf-Hirschhorn est dû à une délétion partielle du bras court du chromosome 4 et plus...

Wolf-Hirschhorn syndrome: A case demonstrated by a cytogenetic study

Pokale, Yamini S.
Jadhav, Ajinkya M.
Kate, Ushang

August 2012

We present a case with a 4p terminal deletion, evidenced in GTG-banded chromosome study. Phenotypic ...

Características clínicas y citogenéticas en el síndrome de Wolf-Hirschhorn. Serie de casos

Cammarata Scalisi, Francisco R.
Callea, Michele
Da Silva, Gloria
Araque, Dionora
Lacruz Rengel, María Angelina

January 2015

Wolf-Hirschhorn syndrome is a genetic entity produced by a partial deletion spanning the distal shor...

Wolf-hirschhorn syndrome: A case study and disease overview

Bailey, Regina

January 2014

Wolf-Hirschhorn syndrome is caused by a deletion of a segment on the short arm (p) of chromosome 4. ...

On the nosology and pathogenesis of Wolf-Hirschhorn syndrome: genotype-phenotype correlation analysis of 80 patients and literature review.

Zollino M
Murdolo M
Marangi G
Pecile V
Galasso C
Neri G.
MAZZANTI, LAURA

January 2008

Based on genotype-phenotype correlation analysis of 80 Wolf-Hirschhorn syndrome (WHS) patients, as w...

Le syndrome de Wolf-Hirschhorn (présence d'une délétion 4p16.3 chez deux jumelles homozygotes et revue de la littérature)

ZARAA, Abdelouahab
MALOU, Etienne

January 2003

Le syndrome de Wolf-Hirschhorn est dû à une délétion partielle du bras court du chromosome 4 et plus...

Wolf-Hirschhorn Syndrome: Clinical and Genetic Study of 7 New Cases, and Mini Review

Eva-Cristiana Gavril
Alina Costina Luca
Alexandrina-Stefania Curpan
Roxana Popescu
Irina Resmerita
Monica Cristina Panzaru
Lacramioara Ionela Butnariu
Eusebiu Vlad Gorduza
Mihaela Gramescu
Cristina Rusu

August 2021

Wolf–Hirschhorn syndrome (WHS), a rare disorder determined by distal 4p deletion, is characterized b...

Pathogenic significance of deletions distal to the currently described Wolf-Hirschhorn syndrome critical regions on 4p16.3

South, Sarah T
Hannes, Femke
Fisch, Gene S
Vermeesch, Joris
Zollino, Marcella

November 2008

Within recent years, numerous individuals have been identified with terminal 4p microdeletions dista...

Wolf-Hirschhorn Syndrome: Clinical and Genetic Data from a First Case Diagnosed in Central Africa.

Mbuyi-Musanzayi, Sebastien
Lumaka Zola, Aimé
Kasole, Toni Lubala
Ilunga, Erick Kasamba
Asani, Bienvenu Yogolelo
Tshilobo, Prosper Lukusa
Muenze, Prosper Kalenga
Reychler, Herve
Katombe, Francois Tshilombo
Devriendt, Koenraad

January 2017

peer reviewedWolf-Hirschhorn syndrome (WHS) is a multiple congenital anomaly-intellectual disability...

Hindawi Publishing Corporation Case Reports in Genetics

Article Id

August 2016

Copyright © 2012 F. Sheth et al. This is an open access article distributed under the Creative Commo...

Genotype-phenotype correlations and clinical diagnostic criteria in Wolf-Hirschhorn syndrome

Zollino, Marcella (ORCID:0000-0003-4871-9519)
Di Stefano, C
Zampino, Giuseppe (ORCID:0000-0003-3865-3253)
Mastroiacovo, Pierpaolo
Wright, Tj
Sorge, G
Selicorni, A
Tenconi, Romano
Zappalà, A
Battaglia, Alessandra
Di Rocco, M
Palka, G
Pallotta, R
Altherr, Mr
Neri, Giovanni

January 2000

We report on a clinical-genetic study of 16 Wolf-Hirschhorn syndrome (WHS) patients. Hemizygosity of...

Pathogenic significance of deletions distal to the currently described Wolf-Hirschhorn syndrome critical regions on 4p16.3.

South, Sarah
Hannes, Femke
Fisch, Gene
Vermeesch, Joris Robert
Zollino, Marcella (ORCID:0000-0003-4871-9519)

January 2008

Within recent years, numerous individuals have been identified with terminal 4p microdeletions dista...

Wolf-Hirschhorn syndrome due to pure and translocation forms of monosomy 4p16.1 → pter

Iwanowski, Piotr S
Panasiuk, Barbara
Van Buggenhout, Griet
Murdolo, Marina
Myśliwiec, Marta
Maas, Nicole MC
Lattante, Serena
Korniszewski, Lech
Posmyk, Renata
Pilch, Jacek
Zajączek, Stanislaw
Fryns, Jean-Pierre
Zollino, Marcella
Midro, Alina T

August 2011

The aim of this study was to obtain a quantitative definition of Wolf-Hirschhorn syndrome (WHS) thro...

Wolf-Hirschhorn (4p-) syndrome: Prenatal diagnosis, molecular cytogenetic characterization and association with a 1.2-Mb microduplication at 8p22-p21.3 and a 1.1-Mb microduplication at 10p15.3 in a fetus with an apparently pure 4p deletion

Chen, Chih-Ping
Su, Yi-Ning
Chen, Yi-Yung
Su, Jun-Wei
Chern, Schu-Rern
Chen, Yu-Ting
Chen, Wen-Lin
Chen, Li-Feng
Wang, Wayseen

December 2011

AbstractObjectiveTo present prenatal diagnosis and molecular cytogenetic characterization of Wolf-Hi...

Wolf-Hirschhorn syndrome revealed by status epilepticus: A case report

IMANE FILALI
HABIBA EL YATIM
ABDELILAH RADI
RACHID ABILKACEM
AOMAR AGADR

January 2023

A Wolf-Hirschhorn syndrome is a rare chromosomal anomaly, which results from a deletion of the dista...

Syndrome de Wolf Hirschhorn à propos d’un cas

RAQUI, Aniss

January 2012

le syndrome de Wolf-Hirschhorn est dû à une délétion partielle du bras court du chromosome 4 et plus...

Wolf-Hirschhorn syndrome: A case demonstrated by a cytogenetic study

Pokale, Yamini S.
Jadhav, Ajinkya M.
Kate, Ushang

August 2012

We present a case with a 4p terminal deletion, evidenced in GTG-banded chromosome study. Phenotypic ...

Características clínicas y citogenéticas en el síndrome de Wolf-Hirschhorn. Serie de casos

Cammarata Scalisi, Francisco R.
Callea, Michele
Da Silva, Gloria
Araque, Dionora
Lacruz Rengel, María Angelina

January 2015

Wolf-Hirschhorn syndrome is a genetic entity produced by a partial deletion spanning the distal shor...

Wolf-hirschhorn syndrome: A case study and disease overview

Bailey, Regina

January 2014

Wolf-Hirschhorn syndrome is caused by a deletion of a segment on the short arm (p) of chromosome 4. ...

On the nosology and pathogenesis of Wolf-Hirschhorn syndrome: genotype-phenotype correlation analysis of 80 patients and literature review.

Zollino M
Murdolo M
Marangi G
Pecile V
Galasso C
Neri G.
MAZZANTI, LAURA

January 2008

Based on genotype-phenotype correlation analysis of 80 Wolf-Hirschhorn syndrome (WHS) patients, as w...

Le syndrome de Wolf-Hirschhorn (présence d'une délétion 4p16.3 chez deux jumelles homozygotes et revue de la littérature)

ZARAA, Abdelouahab
MALOU, Etienne

January 2003

Le syndrome de Wolf-Hirschhorn est dû à une délétion partielle du bras court du chromosome 4 et plus...

Wolf-Hirschhorn Syndrome: Clinical and Genetic Study of 7 New Cases, and Mini Review

Eva-Cristiana Gavril
Alina Costina Luca
Alexandrina-Stefania Curpan
Roxana Popescu
Irina Resmerita
Monica Cristina Panzaru
Lacramioara Ionela Butnariu
Eusebiu Vlad Gorduza
Mihaela Gramescu
Cristina Rusu

August 2021

Wolf–Hirschhorn syndrome (WHS), a rare disorder determined by distal 4p deletion, is characterized b...

Pathogenic significance of deletions distal to the currently described Wolf-Hirschhorn syndrome critical regions on 4p16.3

South, Sarah T
Hannes, Femke
Fisch, Gene S
Vermeesch, Joris
Zollino, Marcella

November 2008

Within recent years, numerous individuals have been identified with terminal 4p microdeletions dista...

Wolf-Hirschhorn Syndrome: Clinical and Genetic Data from a First Case Diagnosed in Central Africa.

Mbuyi-Musanzayi, Sebastien
Lumaka Zola, Aimé
Kasole, Toni Lubala
Ilunga, Erick Kasamba
Asani, Bienvenu Yogolelo
Tshilobo, Prosper Lukusa
Muenze, Prosper Kalenga
Reychler, Herve
Katombe, Francois Tshilombo
Devriendt, Koenraad

January 2017

peer reviewedWolf-Hirschhorn syndrome (WHS) is a multiple congenital anomaly-intellectual disability...

Hindawi Publishing Corporation Case Reports in Genetics

Article Id

August 2016

Copyright © 2012 F. Sheth et al. This is an open access article distributed under the Creative Commo...

Genotype-phenotype correlations and clinical diagnostic criteria in Wolf-Hirschhorn syndrome

Zollino, Marcella (ORCID:0000-0003-4871-9519)
Di Stefano, C
Zampino, Giuseppe (ORCID:0000-0003-3865-3253)
Mastroiacovo, Pierpaolo
Wright, Tj
Sorge, G
Selicorni, A
Tenconi, Romano
Zappalà, A
Battaglia, Alessandra
Di Rocco, M
Palka, G
Pallotta, R
Altherr, Mr
Neri, Giovanni

January 2000

We report on a clinical-genetic study of 16 Wolf-Hirschhorn syndrome (WHS) patients. Hemizygosity of...

Pathogenic significance of deletions distal to the currently described Wolf-Hirschhorn syndrome critical regions on 4p16.3.

South, Sarah
Hannes, Femke
Fisch, Gene
Vermeesch, Joris Robert
Zollino, Marcella (ORCID:0000-0003-4871-9519)

January 2008

Within recent years, numerous individuals have been identified with terminal 4p microdeletions dista...

Wolf-Hirschhorn syndrome due to pure and translocation forms of monosomy 4p16.1 → pter

Iwanowski, Piotr S
Panasiuk, Barbara
Van Buggenhout, Griet
Murdolo, Marina
Myśliwiec, Marta
Maas, Nicole MC
Lattante, Serena
Korniszewski, Lech
Posmyk, Renata
Pilch, Jacek
Zajączek, Stanislaw
Fryns, Jean-Pierre
Zollino, Marcella
Midro, Alina T

August 2011

The aim of this study was to obtain a quantitative definition of Wolf-Hirschhorn syndrome (WHS) thro...

Wolf-Hirschhorn (4p-) syndrome: Prenatal diagnosis, molecular cytogenetic characterization and association with a 1.2-Mb microduplication at 8p22-p21.3 and a 1.1-Mb microduplication at 10p15.3 in a fetus with an apparently pure 4p deletion

Chen, Chih-Ping
Su, Yi-Ning
Chen, Yi-Yung
Su, Jun-Wei
Chern, Schu-Rern
Chen, Yu-Ting
Chen, Wen-Lin
Chen, Li-Feng
Wang, Wayseen

December 2011

AbstractObjectiveTo present prenatal diagnosis and molecular cytogenetic characterization of Wolf-Hi...

Wolf-Hirschhorn syndrome revealed by status epilepticus: A case report

IMANE FILALI
HABIBA EL YATIM
ABDELILAH RADI
RACHID ABILKACEM
AOMAR AGADR

January 2023

A Wolf-Hirschhorn syndrome is a rare chromosomal anomaly, which results from a deletion of the dista...

Syndrome de Wolf Hirschhorn à propos d’un cas

RAQUI, Aniss

January 2012

le syndrome de Wolf-Hirschhorn est dû à une délétion partielle du bras court du chromosome 4 et plus...