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Ring chromosome 4 and Wolf–Hirschhorn syndrome (WHS) in a child with multiple anomalies
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| Zeitschriftentitel: | American Journal of Medical Genetics Part A |
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| Personen und Körperschaften: | , , , , , , , |
| In: | American Journal of Medical Genetics Part A, 140A, 2006, 6, S. 628-632 |
| Format: | E-Article |
| Sprache: | Englisch |
| veröffentlicht: |
Wiley
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| Schlagwörter: |
| author_facet |
Balcı, Sevim Engiz, Özlem Aktaş, Dilek Vargel, Ibrahim Beksaç, M.S. Mrasek, Kristin Vermeesch, Joris Liehr, Thomas Balcı, Sevim Engiz, Özlem Aktaş, Dilek Vargel, Ibrahim Beksaç, M.S. Mrasek, Kristin Vermeesch, Joris Liehr, Thomas |
|---|---|
| author |
Balcı, Sevim Engiz, Özlem Aktaş, Dilek Vargel, Ibrahim Beksaç, M.S. Mrasek, Kristin Vermeesch, Joris Liehr, Thomas |
| spellingShingle |
Balcı, Sevim Engiz, Özlem Aktaş, Dilek Vargel, Ibrahim Beksaç, M.S. Mrasek, Kristin Vermeesch, Joris Liehr, Thomas American Journal of Medical Genetics Part A Ring chromosome 4 and Wolf–Hirschhorn syndrome (WHS) in a child with multiple anomalies Genetics (clinical) Genetics |
| author_sort |
balcı, sevim |
| spelling |
Balcı, Sevim Engiz, Özlem Aktaş, Dilek Vargel, Ibrahim Beksaç, M.S. Mrasek, Kristin Vermeesch, Joris Liehr, Thomas 1552-4825 1552-4833 Wiley Genetics (clinical) Genetics http://dx.doi.org/10.1002/ajmg.a.31131 <jats:title>Abstract</jats:title><jats:p>We report on a 16‐month‐old male patient with ring chromosome 4 and deletion of Wolf–Hirschhorn syndrome (WHS) region with multiple congenital anomalies including unilateral cleft lip and palate, iris coloboma, microcephaly, midgut malrotation, hypospadias, and double urethral orifices. Peripheral chromosome analysis of the patient showed 46,XY,r(4)(p16.3q35) de novo. Multicolor fluorescence in situ hybridization (FISH) study was also performed and according to multicolor banding (MCB) a r(4)(::p16.3 → q34.3 ∼ 35.1::) was found in all metaphases. Subtelomeric 4p region, subtelomeric 4q region, as well as, Wolf–Hirschhorn critical region were deleted in ring chromosome 4. Genomic microarray analysis was also performed to delineate the size of deletion. Cranial magnetic resonance imaging (MRI) showed hypoplastic corpus callosum, delayed myelinization, and frontal and occipital lobe atrophies. Both maternal and paternal chromosomal analyses were normal. We compare the phenotypic appearance of our patient with the previously reported 16 cases of ring chromosome 4 in the medical literature. © 2006 Wiley‐Liss, Inc.</jats:p> Ring chromosome 4 and Wolf–Hirschhorn syndrome (WHS) in a child with multiple anomalies American Journal of Medical Genetics Part A |
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Ring chromosome 4 and Wolf–Hirschhorn syndrome (WHS) in a child with multiple anomalies |
| title_unstemmed |
Ring chromosome 4 and Wolf–Hirschhorn syndrome (WHS) in a child with multiple anomalies |
| title_full |
Ring chromosome 4 and Wolf–Hirschhorn syndrome (WHS) in a child with multiple anomalies |
| title_fullStr |
Ring chromosome 4 and Wolf–Hirschhorn syndrome (WHS) in a child with multiple anomalies |
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Ring chromosome 4 and Wolf–Hirschhorn syndrome (WHS) in a child with multiple anomalies |
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Ring chromosome 4 and Wolf–Hirschhorn syndrome (WHS) in a child with multiple anomalies |
| title_sort |
ring chromosome 4 and wolf–hirschhorn syndrome (whs) in a child with multiple anomalies |
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Genetics (clinical) Genetics |
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http://dx.doi.org/10.1002/ajmg.a.31131 |
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2006 |
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628-632 |
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<jats:title>Abstract</jats:title><jats:p>We report on a 16‐month‐old male patient with ring chromosome 4 and deletion of Wolf–Hirschhorn syndrome (WHS) region with multiple congenital anomalies including unilateral cleft lip and palate, iris coloboma, microcephaly, midgut malrotation, hypospadias, and double urethral orifices. Peripheral chromosome analysis of the patient showed 46,XY,r(4)(p16.3q35) de novo. Multicolor fluorescence in situ hybridization (FISH) study was also performed and according to multicolor banding (MCB) a r(4)(::p16.3 → q34.3 ∼ 35.1::) was found in all metaphases. Subtelomeric 4p region, subtelomeric 4q region, as well as, Wolf–Hirschhorn critical region were deleted in ring chromosome 4. Genomic microarray analysis was also performed to delineate the size of deletion. Cranial magnetic resonance imaging (MRI) showed hypoplastic corpus callosum, delayed myelinization, and frontal and occipital lobe atrophies. Both maternal and paternal chromosomal analyses were normal. We compare the phenotypic appearance of our patient with the previously reported 16 cases of ring chromosome 4 in the medical literature. © 2006 Wiley‐Liss, Inc.</jats:p> |
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| author | Balcı, Sevim, Engiz, Özlem, Aktaş, Dilek, Vargel, Ibrahim, Beksaç, M.S., Mrasek, Kristin, Vermeesch, Joris, Liehr, Thomas |
| author_facet | Balcı, Sevim, Engiz, Özlem, Aktaş, Dilek, Vargel, Ibrahim, Beksaç, M.S., Mrasek, Kristin, Vermeesch, Joris, Liehr, Thomas, Balcı, Sevim, Engiz, Özlem, Aktaş, Dilek, Vargel, Ibrahim, Beksaç, M.S., Mrasek, Kristin, Vermeesch, Joris, Liehr, Thomas |
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| description | <jats:title>Abstract</jats:title><jats:p>We report on a 16‐month‐old male patient with ring chromosome 4 and deletion of Wolf–Hirschhorn syndrome (WHS) region with multiple congenital anomalies including unilateral cleft lip and palate, iris coloboma, microcephaly, midgut malrotation, hypospadias, and double urethral orifices. Peripheral chromosome analysis of the patient showed 46,XY,r(4)(p16.3q35) de novo. Multicolor fluorescence in situ hybridization (FISH) study was also performed and according to multicolor banding (MCB) a r(4)(::p16.3 → q34.3 ∼ 35.1::) was found in all metaphases. Subtelomeric 4p region, subtelomeric 4q region, as well as, Wolf–Hirschhorn critical region were deleted in ring chromosome 4. Genomic microarray analysis was also performed to delineate the size of deletion. Cranial magnetic resonance imaging (MRI) showed hypoplastic corpus callosum, delayed myelinization, and frontal and occipital lobe atrophies. Both maternal and paternal chromosomal analyses were normal. We compare the phenotypic appearance of our patient with the previously reported 16 cases of ring chromosome 4 in the medical literature. © 2006 Wiley‐Liss, Inc.</jats:p> |
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| spelling | Balcı, Sevim Engiz, Özlem Aktaş, Dilek Vargel, Ibrahim Beksaç, M.S. Mrasek, Kristin Vermeesch, Joris Liehr, Thomas 1552-4825 1552-4833 Wiley Genetics (clinical) Genetics http://dx.doi.org/10.1002/ajmg.a.31131 <jats:title>Abstract</jats:title><jats:p>We report on a 16‐month‐old male patient with ring chromosome 4 and deletion of Wolf–Hirschhorn syndrome (WHS) region with multiple congenital anomalies including unilateral cleft lip and palate, iris coloboma, microcephaly, midgut malrotation, hypospadias, and double urethral orifices. Peripheral chromosome analysis of the patient showed 46,XY,r(4)(p16.3q35) de novo. Multicolor fluorescence in situ hybridization (FISH) study was also performed and according to multicolor banding (MCB) a r(4)(::p16.3 → q34.3 ∼ 35.1::) was found in all metaphases. Subtelomeric 4p region, subtelomeric 4q region, as well as, Wolf–Hirschhorn critical region were deleted in ring chromosome 4. Genomic microarray analysis was also performed to delineate the size of deletion. Cranial magnetic resonance imaging (MRI) showed hypoplastic corpus callosum, delayed myelinization, and frontal and occipital lobe atrophies. Both maternal and paternal chromosomal analyses were normal. We compare the phenotypic appearance of our patient with the previously reported 16 cases of ring chromosome 4 in the medical literature. © 2006 Wiley‐Liss, Inc.</jats:p> Ring chromosome 4 and Wolf–Hirschhorn syndrome (WHS) in a child with multiple anomalies American Journal of Medical Genetics Part A |
| spellingShingle | Balcı, Sevim, Engiz, Özlem, Aktaş, Dilek, Vargel, Ibrahim, Beksaç, M.S., Mrasek, Kristin, Vermeesch, Joris, Liehr, Thomas, American Journal of Medical Genetics Part A, Ring chromosome 4 and Wolf–Hirschhorn syndrome (WHS) in a child with multiple anomalies, Genetics (clinical), Genetics |
| title | Ring chromosome 4 and Wolf–Hirschhorn syndrome (WHS) in a child with multiple anomalies |
| title_full | Ring chromosome 4 and Wolf–Hirschhorn syndrome (WHS) in a child with multiple anomalies |
| title_fullStr | Ring chromosome 4 and Wolf–Hirschhorn syndrome (WHS) in a child with multiple anomalies |
| title_full_unstemmed | Ring chromosome 4 and Wolf–Hirschhorn syndrome (WHS) in a child with multiple anomalies |
| title_short | Ring chromosome 4 and Wolf–Hirschhorn syndrome (WHS) in a child with multiple anomalies |
| title_sort | ring chromosome 4 and wolf–hirschhorn syndrome (whs) in a child with multiple anomalies |
| title_unstemmed | Ring chromosome 4 and Wolf–Hirschhorn syndrome (WHS) in a child with multiple anomalies |
| topic | Genetics (clinical), Genetics |
| url | http://dx.doi.org/10.1002/ajmg.a.31131 |