Literature DB >> 6759367

The dermatoglyphic and clinical features of the 9p trisomy and partial 9p monosomy syndromes.

R S Young, T Reed, M E Hodes, C G Palmer.   

Abstract

The physical and dermatoglyphic features obtained from published reports of 128 patients with the trisomy 9p syndrome and 27 patients with the partial 9p monosomy syndrome are tabulated. This information is also provided on two new individuals with each of these chromosomal disorders. The dermal ridge patterns and palmar creases of trisomy 9p which are most helpful from a diagnostic standpoint are zygodactylous or absent palmar digital triradii, brachymesophalangy, reduced total finger ridge count, complex thenar/ID I patterns, transverse palmar ridge alignment, simian creases, distal axial triradii, and great toe and hallucal arch patterns. The characteristic features in partial 9p monosomy include dolichomesophalangy with accessory finger flexion creases, digital whorl patterns and elevated total finger ridge count, distal axial triradii, simian creases, and palmar dermal ridge dissociation.

Entities:  

Mesh:

Year:  1982        PMID: 6759367     DOI: 10.1007/bf00295601

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  10 in total

1.  The simian and Sydney crease.

Authors:  W Wertelecki
Journal:  Birth Defects Orig Artic Ser       Date:  1979

2.  A case of 9p- syndrome.

Authors:  Y Kuroki; S Yokota; H Nakai; Y Yamamoto; I Matsui
Journal:  Hum Genet       Date:  1977-08-31       Impact factor: 4.132

3.  The deletion 9p syndrome. A 61-year-old man with deletion of short arm 9.

Authors:  J Nielsen; A Homma; F Christiansen; K Rasmussen; P Saldaña-Garcia
Journal:  Clin Genet       Date:  1977-08       Impact factor: 4.438

4.  A case of partial 9p monosomy with some unusual clinical features.

Authors:  F J Rutten; T W Hustinx; A A Dunk-Tillemans; J M Scheres; Y S Tjon
Journal:  Ann Genet       Date:  1978-03

5.  Dermatoglyphic sole patterns. a new attempt at classification.

Authors:  L S Penrose; D Loesch
Journal:  Hum Biol       Date:  1969-09       Impact factor: 0.553

6.  Topological classification of palmar dermatoglyphics.

Authors:  L S Penrose; D Loesch
Journal:  J Ment Defic Res       Date:  1970-06

7.  The dermatoglyphic pattern of the trisomy 9p syndrome.

Authors:  A Rodewald; S Stengel-Rutkowski; M Zankl
Journal:  Clin Genet       Date:  1979-12       Impact factor: 4.438

8.  Dermatoglyphic patterns in 9p trisomy syndrome.

Authors:  D Loesch; J Czyzewska
Journal:  J Ment Defic Res       Date:  1978-03

Review 9.  Dermatoglyphics in medicine--problems and use in suspected chromosome abnormalities.

Authors:  T Reed
Journal:  Am J Med Genet       Date:  1981

10.  Nonrandom distribution of exchange points in patients with reciprocal translocations.

Authors:  C Stoll
Journal:  Hum Genet       Date:  1980       Impact factor: 4.132

  10 in total
  11 in total

1.  Chromosome breakage hotspots and delineation of the critical region for the 9p-deletion syndrome.

Authors:  L A Christ; C A Crowe; M A Micale; J M Conroy; S Schwartz
Journal:  Am J Hum Genet       Date:  1999-11       Impact factor: 11.025

2.  A mild phenotype associated with der(9)t(3;9) (p25;p23).

Authors:  R J McClure; N Telford; S J Newell
Journal:  J Med Genet       Date:  1996-07       Impact factor: 6.318

3.  Molecular cytogenetic characterisation of the first familial case of partial 9p duplication (p22p24).

Authors:  B R Haddad; A E Lin; H Wyandt; A Milunsky
Journal:  J Med Genet       Date:  1996-12       Impact factor: 6.318

Review 4.  Eleven new cases of del(9p) and features from 80 cases.

Authors:  J L Huret; C Leonard; B Forestier; M O Rethoré; J Lejeune
Journal:  J Med Genet       Date:  1988-11       Impact factor: 6.318

5.  Deletion 9p and sex reversal.

Authors:  C P Bennett; Z Docherty; S A Robb; P Ramani; J R Hawkins; D Grant
Journal:  J Med Genet       Date:  1993-06       Impact factor: 6.318

6.  Demonstration of gene dosage effects for AK3 and GALT in fibroblasts from a fetus with 9p trisomy.

Authors:  P Steinbach; R Benz
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

7.  Molecular genetic analysis of partial 9p trisomy in two Chinese families with mental retardation and facial anomaly.

Authors:  Aiping Feng; Xiaohua Dai; Xiaoran Wang; Yong Gao; Ruili Luo; Yulei Li; Na Zhang; Jingyu Liu
Journal:  J Huazhong Univ Sci Technolog Med Sci       Date:  2011-08-07

8.  De novo tandem duplication 9p (p12----p24) with normal GALT activity in red cells.

Authors:  T Motegi; K Watanabe; N Nakamura; T Hasegawa; Y Yanagawa
Journal:  J Med Genet       Date:  1985-02       Impact factor: 6.318

9.  De Novo Duplication of Chromosome 9p in a Female Infant: Phenotype and Genotype Correlation.

Authors:  Paola E Leone; Andy Pérez-Villa; Verónica Yumiceba; María Ángeles Hernández; Jennyfer M García-Cárdenas; Isaac Armendáriz-Castillo; Santiago Guerrero; Patricia Guevara-Ramírez; Andrés López-Cortés; Ana Karina Zambrano; Juan Luis García; Jesús María Hernández; César Paz-Y-Miño
Journal:  J Pediatr Genet       Date:  2019-09-16

10.  Heterozygous mutations of FREM1 are associated with an increased risk of isolated metopic craniosynostosis in humans and mice.

Authors:  Lisenka E L M Vissers; Timothy C Cox; A Murat Maga; Kieran M Short; Fenny Wiradjaja; Irene M Janssen; Fernanda Jehee; Debora Bertola; Jia Liu; Garima Yagnik; Kiyotoshi Sekiguchi; Daiji Kiyozumi; Hans van Bokhoven; Carlo Marcelis; Michael L Cunningham; Peter J Anderson; Simeon A Boyadjiev; Maria Rita Passos-Bueno; Joris A Veltman; Ian Smyth; Michael F Buckley; Tony Roscioli
Journal:  PLoS Genet       Date:  2011-09-08       Impact factor: 5.917

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