Literature DB >> 14684683

Identification of a locus for type I punctate palmoplantar keratoderma on chromosome 15q22-q24.

A Martinez-Mir1, A Zlotogorski, D Londono, D Gordon, A Grunn, E Uribe, L Horev, I M Ruiz, N O Davalos, O Alayan, J Liu, T C Gilliam, J C Salas-Alanis, A M Christiano.   

Abstract

BACKGROUND: The identification of the molecular basis of disorders of keratinisation has significantly advanced our understanding of skin biology, revealing new information on key structures in the skin, such as the intermediate filaments, desmosomes, and gap junctions. Among these disorders, there is an extraordinarily heterogeneous group known as palmoplantar keratodermas (PPK), for which only a few molecular defects have been described. A particular form of PPK, known as punctate PPK, has been described in a few large autosomal dominant pedigrees, but its genetic basis has yet to be identified. AIM: Identification of the gene for punctate PPK.
METHODS: Clinical examination and linkage analysis in three families with punctate PPK.
RESULTS: A genomewide scan was performed on an extended autosomal dominant pedigree, and linkage to chromosome 15q22-q24 was identified. With the addition of two new families with the same phenotype, we confirmed the mapping of the locus for punctate PPK to a 9.98 cM interval, flanked by markers D15S534 and D15S818 (maximum two point lod score of 4.93 at theta = 0 for marker D15S988).
CONCLUSIONS: We report the clinical and genetic findings in three pedigrees with the punctate form of PPK. We have mapped a genetic locus for this phenotype to chromosome 15q22-q24, which indicates the identification of a new gene involved in skin integrity.

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Year:  2003        PMID: 14684683      PMCID: PMC1735333          DOI: 10.1136/jmg.40.12.872

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  53 in total

1.  Genomewide linkage analysis of celiac disease in Finnish families.

Authors:  Jianjun Liu; Suh-Hang Juo; Päivi Holopainen; Joseph Terwilliger; Xiaomei Tong; Adina Grunn; Miguel Brito; Peter Green; Kirsi Mustalahti; Markku Mäki; T Conrad Gilliam; Jukka Partanen
Journal:  Am J Hum Genet       Date:  2001-11-19       Impact factor: 11.025

Review 2.  SPINK5: both rare and common skin disease.

Authors:  Elizabeth E Norgett; David P Kelsell
Journal:  Trends Mol Med       Date:  2002-01       Impact factor: 11.951

3.  Evidence for extensive locus heterogeneity in Naxos disease.

Authors:  Karima Djabali; Amalia Martinez-Mir; Liran Horev; Angela M Christiano; Abraham Zlotogorski
Journal:  J Invest Dermatol       Date:  2002-03       Impact factor: 8.551

4.  47 patients in 14 families with the rare genodermatosis keratosis punctata palmoplantaris Buschke-Fischer-Brauer.

Authors:  Steffen Emmert; Wolfgang Küster; Hans-Christian Hennies; Markus Zutt; Holger Haenssle; Lutz Kretschmer; Christine Neumann
Journal:  Eur J Dermatol       Date:  2003 Jan-Feb       Impact factor: 3.328

5.  A high-resolution recombination map of the human genome.

Authors:  Augustine Kong; Daniel F Gudbjartsson; Jesus Sainz; Gudrun M Jonsdottir; Sigurjon A Gudjonsson; Bjorgvin Richardsson; Sigrun Sigurdardottir; John Barnard; Bjorn Hallbeck; Gisli Masson; Adam Shlien; Stefan T Palsson; Michael L Frigge; Thorgeir E Thorgeirsson; Jeffrey R Gulcher; Kari Stefansson
Journal:  Nat Genet       Date:  2002-06-10       Impact factor: 38.330

6.  Carcinoma of the oesophagus with keratosis palmaris et plantaris (tylosis): a study of two families.

Authors:  W HOWEL-EVANS; R B McCONNELL; C A CLARKE; P M SHEPPARD
Journal:  Q J Med       Date:  1958-07

7.  Compound heterozygosity for non-sense and mis-sense mutations in desmoplakin underlies skin fragility/woolly hair syndrome.

Authors:  Neil V Whittock; Hong Wan; Susan M Morley; Maria C Garzon; Leonard Kristal; Patrice Hyde; W H Irwin McLean; Leena Pulkkinen; Juoni Uitto; Angela M Christiano; Robin A J Eady; John A McGrath
Journal:  J Invest Dermatol       Date:  2002-02       Impact factor: 8.551

Review 8.  Structural and functional diversity of lysyl oxidase and the LOX-like proteins.

Authors:  J Molnar; K S K Fong; Q P He; K Hayashi; Y Kim; S F T Fong; B Fogelgren; K Molnarne Szauter; M Mink; K Csiszar
Journal:  Biochim Biophys Acta       Date:  2003-04-11

9.  Gene polymorphism in Netherton and common atopic disease.

Authors:  A J Walley; S Chavanas; M F Moffatt; R M Esnouf; B Ubhi; R Lawrence; K Wong; G R Abecasis; E Y Jones; J I Harper; A Hovnanian; W O Cookson
Journal:  Nat Genet       Date:  2001-10       Impact factor: 38.330

Review 10.  The molecular basis of hereditary palmoplantar keratodermas.

Authors:  Arash Kimyai-Asadi; Lauren B Kotcher; Ming H Jih
Journal:  J Am Acad Dermatol       Date:  2002-09       Impact factor: 11.527

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  7 in total

Review 1.  Factors affecting statistical power in the detection of genetic association.

Authors:  Derek Gordon; Stephen J Finch
Journal:  J Clin Invest       Date:  2005-06       Impact factor: 14.808

2.  Whole-exome sequencing analysis reveals co-segregation of a COL20A1 missense mutation in a Pakistani family with striate palmoplantar keratoderma.

Authors:  Muhammad Ismail Khan; Soyeon Choi; Muhammad Zahid; Habib Ahmad; Roshan Ali; Musharraf Jelani; Changsoo Kang
Journal:  Genes Genomics       Date:  2018-05-02       Impact factor: 1.839

3.  Nonsense mutations in AAGAB cause punctate palmoplantar keratoderma type Buschke-Fischer-Brauer.

Authors:  Kathrin A Giehl; Gertrud N Eckstein; Sandra M Pasternack; Silke Praetzel-Wunder; Thomas Ruzicka; Peter Lichtner; Kerstin Seidl; Mike Rogers; Elisabeth Graf; Lutz Langbein; Markus Braun-Falco; Regina C Betz; Tim M Strom
Journal:  Am J Hum Genet       Date:  2012-09-20       Impact factor: 11.025

4.  Heterozygous mutations in AAGAB cause type 1 punctate palmoplantar keratoderma with evidence for increased growth factor signaling.

Authors:  Elizabeth Pöhler; Mozheh Zamiri; Catriona P Harkins; Julio C Salas-Alanis; William Perkins; Frances J D Smith; W H Irwin McLean; Sara J Brown
Journal:  J Invest Dermatol       Date:  2013-06-06       Impact factor: 8.551

5.  Identification of distinct mutations in AAGAB in families with type 1 punctate palmoplantar keratoderma.

Authors:  Megan Furniss; Claire A Higgins; Amalia Martinez-Mir; Liran Horev; Lynn Petukhova; Andrija Stanimirović; Jovan Miljković; Abraham Zlotogorski; Angela M Christiano
Journal:  J Invest Dermatol       Date:  2014-01-03       Impact factor: 8.551

6.  Haploinsufficiency for AAGAB causes clinically heterogeneous forms of punctate palmoplantar keratoderma.

Authors:  Elizabeth Pohler; Ons Mamai; Jennifer Hirst; Mozheh Zamiri; Helen Horn; Toshifumi Nomura; Alan D Irvine; Benvon Moran; Neil J Wilson; Frances J D Smith; Christabelle S M Goh; Aileen Sandilands; Christian Cole; Geoffrey J Barton; Alan T Evans; Hiroshi Shimizu; Masashi Akiyama; Mitsuhiro Suehiro; Izumi Konohana; Mohammad Shboul; Sebastien Teissier; Lobna Boussofara; Mohamed Denguezli; Ali Saad; Moez Gribaa; Patricia J Dopping-Hepenstal; John A McGrath; Sara J Brown; David R Goudie; Bruno Reversade; Colin S Munro; W H Irwin McLean
Journal:  Nat Genet       Date:  2012-10-14       Impact factor: 38.330

7.  New and recurrent AAGAB mutations in punctate palmoplantar keratoderma.

Authors:  E Pohler; M Huber; S E Boonen; M Zamiri; P A Gregersen; M Sommerlund; M Ramsing; D Hohl; W H I McLean; F J D Smith
Journal:  Br J Dermatol       Date:  2014-08-07       Impact factor: 9.302

  7 in total

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