Literature DB >> 21800331

High-risk pregnancy and neonatal complications in the DNA repair and transcription disorder trichothiodystrophy: report of 27 affected pregnancies.

Deborah Tamura1, Melissa Merideth, John J DiGiovanna, Xiaolong Zhou, Margaret A Tucker, Alisa M Goldstein, Brian P Brooks, Sikandar G Khan, Kyu-Seon Oh, Takahiro Ueda, Jennifer Boyle, Roxana Moslehi, Kenneth H Kraemer.   

Abstract

OBJECTIVE: To identify the frequency of pregnancy and neonatal complications in pregnancies carrying fetuses affected with trichothiodystrophy (TTD).
METHODS: We identified pregnancy and neonatal complications and serum screening results from mothers of TTD patients in a DNA repair diseases study from 2001 to 2011.
RESULTS: Pregnancy reports of 27 TTD patients and their 23 mothers were evaluated and 81% of the pregnancies had complications: 56% had preterm delivery, 30% had preeclampsia, 19% had placental abnormalities, 11% had HELLP syndrome, and 4% had an emergency c-section for fetal distress, while 44% had two or more complications. Only 19% of the pregnancies delivered at term without complications. Eight of the ten pregnancies tested had abnormal multiple marker results including elevated levels of human chorionic gonadotrophin. Eighty-five percent of the neonates had complications: 70% were low birth weight (<2500 g), 35% had birth weight < 10 centile for gestational age, 70% had NICU admission, 67% had a collodion membrane, and 31% of the 16 males had cryptorchidism. Cataracts were present in 54% of the TTD patients examined.
CONCLUSION: TTD is a multisystem disease that predisposes mothers of affected patients to substantial risks for pregnancy complications and TTD neonates have a high incidence of multiple abnormalities. Published 2011. This article is a U.S. Government work and is in the public domain in the USA.

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Year:  2011        PMID: 21800331      PMCID: PMC3266696          DOI: 10.1002/pd.2829

Source DB:  PubMed          Journal:  Prenat Diagn        ISSN: 0197-3851            Impact factor:   3.050


  35 in total

1.  Pregnancy outcome and long term prognosis in 868 children born after second trimester amniocentesis for maternal serum positive triple test screening and normal prenatal karyotype.

Authors:  I Witters; E Legius; K Devriendt; P Moerman; D Van Schoubroeck; A Van Assche; J P Fryns
Journal:  J Med Genet       Date:  2001-05       Impact factor: 6.318

2.  Physical and psychomotor development of 1799 children born after second trimester amniocentesis for maternal serum positive triple test screening and normal prenatal karyotype.

Authors:  I Witters; P Moerman; A Van Assche; J-P Fryns
Journal:  J Med Genet       Date:  2002-12       Impact factor: 6.318

3.  Prenatal diagnosis in a subset of trichothiodystrophy patients defective in DNA repair.

Authors:  A Sarasin; C Blanchet-Bardon; G Renault; A Lehmann; C Arlett; Y Dumez
Journal:  Br J Dermatol       Date:  1992-11       Impact factor: 9.302

4.  Second-trimester maternal serum alpha-fetoprotein and risk of adverse pregnancy outcome(1).

Authors:  T G Krause; P Christens; J Wohlfahrt; U Lei; T Westergaard; B Nørgaard-Pedersen; M Melbye
Journal:  Obstet Gynecol       Date:  2001-02       Impact factor: 7.661

Review 5.  Trichothiodystrophy: update on the sulfur-deficient brittle hair syndromes.

Authors:  P H Itin; A Sarasin; M R Pittelkow
Journal:  J Am Acad Dermatol       Date:  2001-06       Impact factor: 11.527

6.  In utero diagnosis of trichothiodystrophy by endoscopically-guided fetal eyebrow biopsy.

Authors:  R A Quintero; W J Morales; E Gilbert-Barness; J Claus; P W Bornick; M H Allen; J Ackerman; B Koussef
Journal:  Fetal Diagn Ther       Date:  2000 May-Jun       Impact factor: 2.587

Review 7.  Pregnancy and inherited metabolic disorders: maternal and fetal complications.

Authors:  Mary Anne Preece; Anne Green
Journal:  Ann Clin Biochem       Date:  2002-09       Impact factor: 2.057

Review 8.  DNA repair-deficient diseases, xeroderma pigmentosum, Cockayne syndrome and trichothiodystrophy.

Authors:  Alan R Lehmann
Journal:  Biochimie       Date:  2003-11       Impact factor: 4.079

9.  Association between second-trimester isolated high maternal serum maternal serum human chorionic gonadotropin levels and obstetric complications in singleton and twin pregnancies.

Authors:  Nathalie Lepage; David Chitayat; John Kingdom; Tianhua Huang
Journal:  Am J Obstet Gynecol       Date:  2003-05       Impact factor: 8.661

10.  Prospective prevention of neonatal hyperammonaemia in argininosuccinic acidura by arginine therapy.

Authors:  S M Donn; J G Thoene
Journal:  J Inherit Metab Dis       Date:  1985       Impact factor: 4.982

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  13 in total

1.  Pregnancy outcomes in mothers of offspring with inherited bone marrow failure syndromes.

Authors:  Neelam Giri; Helen D Reed; Pamela Stratton; Sharon A Savage; Blanche P Alter
Journal:  Pediatr Blood Cancer       Date:  2017-08-12       Impact factor: 3.167

2.  Placental aging and oxidation damage in a tissue micro-array model: an immunohistochemistry study.

Authors:  Ambrogio P Londero; Maria Orsaria; Stefania Marzinotto; Tiziana Grassi; Arrigo Fruscalzo; Angelo Calcagno; Serena Bertozzi; Nastassia Nardini; Enrica Stella; Ralph J Lellé; Lorenza Driul; Gianluca Tell; Laura Mariuzzi
Journal:  Histochem Cell Biol       Date:  2016-04-22       Impact factor: 4.304

3.  Effect of mutations in XPD(ERCC2) on pregnancy and prenatal development in mothers of patients with trichothiodystrophy or xeroderma pigmentosum.

Authors:  Deborah Tamura; Sikandar G Khan; Melissa Merideth; John J DiGiovanna; Margaret A Tucker; Alisa M Goldstein; Kyu-Seon Oh; Takahiro Ueda; Jennifer Boyle; Mansi Sarihan; Kenneth H Kraemer
Journal:  Eur J Hum Genet       Date:  2012-05-23       Impact factor: 4.246

4.  Abnormal XPD-induced nuclear receptor transactivation in DNA repair disorders: trichothiodystrophy and xeroderma pigmentosum.

Authors:  Xiaolong Zhou; Sikandar G Khan; Deborah Tamura; Takahiro Ueda; Jennifer Boyle; Emmanuel Compe; Jean-Marc Egly; John J DiGiovanna; Kenneth H Kraemer
Journal:  Eur J Hum Genet       Date:  2012-12-12       Impact factor: 4.246

5.  Arginine vasopressin infusion is sufficient to model clinical features of preeclampsia in mice.

Authors:  Jeremy A Sandgren; Guorui Deng; Danny W Linggonegoro; Sabrina M Scroggins; Katherine J Perschbacher; Anand R Nair; Taryn E Nishimura; Shao Yang Zhang; Larry N Agbor; Jing Wu; Henry L Keen; Meghan C Naber; Nicole A Pearson; Kathy A Zimmerman; Robert M Weiss; Noelle C Bowdler; Yuriy M Usachev; Donna A Santillan; Matthew J Potthoff; Gary L Pierce; Katherine N Gibson-Corley; Curt D Sigmund; Mark K Santillan; Justin L Grobe
Journal:  JCI Insight       Date:  2018-10-04

6.  Growth and nutrition in children with trichothiodystrophy.

Authors:  Emily C Atkinson; Diana Thiara; Deborah Tamura; John J DiGiovanna; Kenneth H Kraemer; Colleen Hadigan
Journal:  J Pediatr Gastroenterol Nutr       Date:  2014-10       Impact factor: 2.839

7.  Auditory analysis of xeroderma pigmentosum 1971-2012: hearing function, sun sensitivity and DNA repair predict neurological degeneration.

Authors:  Mariam B Totonchy; Deborah Tamura; Matthew S Pantell; Christopher Zalewski; Porcia T Bradford; Saumil N Merchant; Joseph Nadol; Sikandar G Khan; Raphael Schiffmann; Tyler Mark Pierson; Edythe Wiggs; Andrew J Griffith; John J DiGiovanna; Kenneth H Kraemer; Carmen C Brewer
Journal:  Brain       Date:  2013-01       Impact factor: 13.501

Review 8.  Shining a light on xeroderma pigmentosum.

Authors:  John J DiGiovanna; Kenneth H Kraemer
Journal:  J Invest Dermatol       Date:  2012-01-05       Impact factor: 8.551

9.  Mutations in the TTDN1 gene are associated with a distinct trichothiodystrophy phenotype.

Authors:  Elizabeth R Heller; Sikandar G Khan; Christiane Kuschal; Deborah Tamura; John J DiGiovanna; Kenneth H Kraemer
Journal:  J Invest Dermatol       Date:  2014-10-07       Impact factor: 8.551

10.  GTF2E2 Mutations Destabilize the General Transcription Factor Complex TFIIE in Individuals with DNA Repair-Proficient Trichothiodystrophy.

Authors:  Christiane Kuschal; Elena Botta; Donata Orioli; John J Digiovanna; Sara Seneca; Kathelijn Keymolen; Deborah Tamura; Elizabeth Heller; Sikandar G Khan; Giuseppina Caligiuri; Manuela Lanzafame; Tiziana Nardo; Roberta Ricotti; Fiorenzo A Peverali; Robert Stephens; Yongmei Zhao; Alan R Lehmann; Laura Baranello; David Levens; Kenneth H Kraemer; Miria Stefanini
Journal:  Am J Hum Genet       Date:  2016-03-17       Impact factor: 11.025

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