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15q overgrowth syndrome: A newly recognized phenotype associated with overgrowth, learning difficulties, characteristic facial appearance, renal anomalies and increased dosage of distal chromosome 15q

15q overgrowth syndrome: A newly recognized phenotype associated with overgrowth, learning difficulties, characteristic facial appearance, renal anomalies and increased dosage of distal chromosome 15q
15q overgrowth syndrome: A newly recognized phenotype associated with overgrowth, learning difficulties, characteristic facial appearance, renal anomalies and increased dosage of distal chromosome 15q
Trisomy and tetrasomy of distal chromosome 15q have rarely been reported. Although most of the described patients have some learning difficulties and are overgrown, the phenotype associated with distal trisomy/tetrasomy 15q is uncertain due to the small numbers of reported cases and the common co-occurrence of additional chromosome deletions in many patients with trisomy 15q. We present five individuals with overgrowth, learning difficulties and increased dosage of distal 15q. Partial trisomy 15q was identified in four of these cases. Two were generated through recombination of a parental pericentric inversion and two were generated through malsegregation of a maternal balanced 14;15 reciprocal translocation. In all four cases the trisomy can be considered pure as the 14p and 15p monosomies will exert no phenotypic effect. Partial tetrasomy 15q, as the result of an analphoid supernumerary chromosome derived from an inverted duplication of distal 15q, was identified in the fifth patient. In addition to the overgrowth and learning difficulties, all five had a characteristic facial appearance and three had renal anomalies. The gestalt consists of a long, thin face with a prominent chin and nose. Renal anomalies included renal agenesis, horseshoe kidney, and hydronephrosis. We provide further support for a distinct 15q overgrowth syndrome caused by either trisomy or tetrasomy resulting in increased dosage of distal 15q. In addition we propose that renal anomalies and a distinctive facial appearance be considered major features of this conditio
trisomy 15q, tetrasomy 15q, overgrowth, renal anomalies
1552-4825
147-154
Tatton-Brown, Katrina
dbad5eb1-70eb-4fde-8f67-a37ff32ef9c6
Pilz, Daniela T.
b8b45294-b911-4a73-9ffa-edbb7c6486d7
Örstavik, Karen Helen
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Patton, Michael
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Barber, John C.K.
4785a6e4-bd63-4230-ab61-41a0ae12c761
Collinson, Morag N.
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Maloney, Vivienne K.
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Huang, Shuwen
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Crolla, John A.
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Marks, Karen
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Ormerod, Eli
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Thompson, Peter
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Nawaz, Zafar
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Lese-Martin, Chistsa
e375ffe5-0dca-4a11-811f-574c6e2e922f
Tomkins, Susan
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Waits, Paula
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Rahman, Nazneen
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McEntagart, Meriel
4934e0c0-a279-4603-a3a3-8f364e82fbea
Tatton-Brown, Katrina
dbad5eb1-70eb-4fde-8f67-a37ff32ef9c6
Pilz, Daniela T.
b8b45294-b911-4a73-9ffa-edbb7c6486d7
Örstavik, Karen Helen
55db13fe-c936-48fc-95ad-f7aba41ed4c2
Patton, Michael
a798b7cb-03d5-4aaf-bee1-c2e8e1f15f7d
Barber, John C.K.
4785a6e4-bd63-4230-ab61-41a0ae12c761
Collinson, Morag N.
e1313be8-5065-4e8a-a4df-ccf5bf29d466
Maloney, Vivienne K.
b00dc88c-7927-41e4-96cd-f733ee3339af
Huang, Shuwen
44f28908-02b8-46d7-822c-e6a9e7981723
Crolla, John A.
c5f23751-8de9-4a55-9cc5-ca2fb635769c
Marks, Karen
4cd4afe7-758a-4b4b-b1f8-5f1ece33d332
Ormerod, Eli
af38cd87-8be4-4491-ae84-cf61291eb3e1
Thompson, Peter
c12103d9-d46c-464c-8904-5fbaaa499520
Nawaz, Zafar
33bafa63-afb4-40ad-8e0f-4d03c3b91f00
Lese-Martin, Chistsa
e375ffe5-0dca-4a11-811f-574c6e2e922f
Tomkins, Susan
ee6f8f5a-1b40-43d9-a623-f821ef737a05
Waits, Paula
1e12f190-ba37-4e90-899c-1932b9c1cd46
Rahman, Nazneen
d5eded76-0af9-4d72-8fea-84986bf49c51
McEntagart, Meriel
4934e0c0-a279-4603-a3a3-8f364e82fbea

Tatton-Brown, Katrina, Pilz, Daniela T., Örstavik, Karen Helen, Patton, Michael, Barber, John C.K., Collinson, Morag N., Maloney, Vivienne K., Huang, Shuwen, Crolla, John A., Marks, Karen, Ormerod, Eli, Thompson, Peter, Nawaz, Zafar, Lese-Martin, Chistsa, Tomkins, Susan, Waits, Paula, Rahman, Nazneen and McEntagart, Meriel (2009) 15q overgrowth syndrome: A newly recognized phenotype associated with overgrowth, learning difficulties, characteristic facial appearance, renal anomalies and increased dosage of distal chromosome 15q. American Journal of Medical Genetics part A, 149A (2), 147-154. (doi:10.1002/ajmg.a.32534).

Record type: Article

Abstract

Trisomy and tetrasomy of distal chromosome 15q have rarely been reported. Although most of the described patients have some learning difficulties and are overgrown, the phenotype associated with distal trisomy/tetrasomy 15q is uncertain due to the small numbers of reported cases and the common co-occurrence of additional chromosome deletions in many patients with trisomy 15q. We present five individuals with overgrowth, learning difficulties and increased dosage of distal 15q. Partial trisomy 15q was identified in four of these cases. Two were generated through recombination of a parental pericentric inversion and two were generated through malsegregation of a maternal balanced 14;15 reciprocal translocation. In all four cases the trisomy can be considered pure as the 14p and 15p monosomies will exert no phenotypic effect. Partial tetrasomy 15q, as the result of an analphoid supernumerary chromosome derived from an inverted duplication of distal 15q, was identified in the fifth patient. In addition to the overgrowth and learning difficulties, all five had a characteristic facial appearance and three had renal anomalies. The gestalt consists of a long, thin face with a prominent chin and nose. Renal anomalies included renal agenesis, horseshoe kidney, and hydronephrosis. We provide further support for a distinct 15q overgrowth syndrome caused by either trisomy or tetrasomy resulting in increased dosage of distal 15q. In addition we propose that renal anomalies and a distinctive facial appearance be considered major features of this conditio

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Published date: February 2009
Keywords: trisomy 15q, tetrasomy 15q, overgrowth, renal anomalies

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Local EPrints ID: 69643
URI: http://eprints.soton.ac.uk/id/eprint/69643
ISSN: 1552-4825
PURE UUID: fe022440-c78b-4778-9757-53853c03efd9

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Date deposited: 25 Nov 2009
Last modified: 13 Mar 2024 19:40

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Contributors

Author: Katrina Tatton-Brown
Author: Daniela T. Pilz
Author: Karen Helen Örstavik
Author: Michael Patton
Author: John C.K. Barber
Author: Morag N. Collinson
Author: Vivienne K. Maloney
Author: Shuwen Huang
Author: John A. Crolla
Author: Karen Marks
Author: Eli Ormerod
Author: Peter Thompson
Author: Zafar Nawaz
Author: Chistsa Lese-Martin
Author: Susan Tomkins
Author: Paula Waits
Author: Nazneen Rahman
Author: Meriel McEntagart

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