Literature DB >> 7942853

Paternal isodisomy for chromosome 7 is compatible with normal growth and development in a patient with congenital chloride diarrhea.

P Höglund1, C Holmberg, A de la Chapelle, J Kere.   

Abstract

Uniparental disomy for maternal chromosome 7 has been described in three patients with recessive disorders. Short stature in each of these patients has been explained by the effect of imprinting of growth-related genes on maternal chromosome 7. Alternatively, although less likely, all these patients may be homozygous for a rare recessive mutation. Here we report both paternal isodisomy for chromosome 7 and normal growth in a patient with a recessive disorder, congenital chloride diarrhea. She had inherited only paternal alleles at 10 loci and was homozygous for another 10 chromosome 7 loci studied. Her physical status and laboratory tests were normal except for a mild high-frequency sensorineural hearing loss. As the patient has normal stature, it is likely that the paternal chromosome 7 lacks the suggested maternal imprinting effect on growth. Paternal isodisomy for human chromosome 7 may have no phenotypic effect on growth.

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Year:  1994        PMID: 7942853      PMCID: PMC1918292     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  34 in total

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Journal:  Nature       Date:  1989-11-16       Impact factor: 49.962

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Journal:  Am J Hum Genet       Date:  1989-09       Impact factor: 11.025

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Authors:  B M Cattanach; M Kirk
Journal:  Nature       Date:  1985 Jun 6-12       Impact factor: 49.962

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Authors:  J E Spence; R G Perciaccante; G M Greig; H F Willard; D H Ledbetter; J F Hejtmancik; M S Pollack; W E O'Brien; A L Beaudet
Journal:  Am J Hum Genet       Date:  1988-02       Impact factor: 11.025

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  19 in total

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Authors:  M P Hitchins; P Stanier; M A Preece; G E Moore
Journal:  J Med Genet       Date:  2001-12       Impact factor: 6.318

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Authors:  Michael A Preece
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3.  Maternal uniparental disomy of chromosome 1 with reduction to homozygosity of the LAMB3 locus in a patient with Herlitz junctional epidermolysis bullosa.

Authors:  L Pulkkinen; F Bullrich; P Czarnecki; L Weiss; J Uitto
Journal:  Am J Hum Genet       Date:  1997-09       Impact factor: 11.025

4.  The ratio of maternal to paternal UPD associated with recessive diseases.

Authors:  Angela M Vianna-Morgante
Journal:  Hum Genet       Date:  2005-05-14       Impact factor: 4.132

Review 5.  Williams syndrome starts making sense.

Authors:  J Ashkenas
Journal:  Am J Hum Genet       Date:  1996-10       Impact factor: 11.025

Review 6.  New developments in Silver-Russell syndrome and implications for clinical practice.

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Journal:  Epigenomics       Date:  2016-04-12       Impact factor: 4.778

Review 7.  Grb10 and Grb14: enigmatic regulators of insulin action--and more?

Authors:  Lowenna J Holt; Kenneth Siddle
Journal:  Biochem J       Date:  2005-06-01       Impact factor: 3.857

8.  Absence of a paternally inherited FOXP2 gene in developmental verbal dyspraxia.

Authors:  Lars Feuk; Aino Kalervo; Marita Lipsanen-Nyman; Jennifer Skaug; Kazuhiko Nakabayashi; Brenda Finucane; Danielle Hartung; Micheil Innes; Batsheva Kerem; Malgorzata J Nowaczyk; Joseph Rivlin; Wendy Roberts; Lili Senman; Anne Summers; Peter Szatmari; Virginia Wong; John B Vincent; Susan Zeesman; Lucy R Osborne; Janis Oram Cardy; Juha Kere; Stephen W Scherer; Katariina Hannula-Jouppi
Journal:  Am J Hum Genet       Date:  2006-09-27       Impact factor: 11.025

9.  A narrow segment of maternal uniparental disomy of chromosome 7q31-qter in Silver-Russell syndrome delimits a candidate gene region.

Authors:  K Hannula; M Lipsanen-Nyman; T Kontiokari; J Kere
Journal:  Am J Hum Genet       Date:  2000-12-08       Impact factor: 11.025

Review 10.  Prenatal and postnatal growth failure associated with maternal heterodisomy for chromosome 7.

Authors:  S Langlois; S L Yong; R D Wilson; L C Kwong; D K Kalousek
Journal:  J Med Genet       Date:  1995-11       Impact factor: 6.318

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