Phenotypic spectrum of autosomal recessive congenital ichthyosis due to PNPLA1 mutation

被引:20
|
作者
Boyden, L. M. [1 ]
Craiglow, B. G. [2 ,3 ]
Hu, R. H. [2 ]
Zhou, J. [2 ]
Browning, J. [5 ]
Eichenfield, L. [6 ]
Lim, Y. L. [7 ]
Luu, M. [8 ]
Randolph, L. M. [9 ]
Ginarte, M. [10 ]
Fachal, L. [11 ]
Rodriguez-Pazos, L. [12 ]
Vega, A. [11 ]
Kramer, D. [13 ]
Yosipovitch, G. [14 ]
Vahidnezhad, H. [15 ]
Youssefian, L. [15 ]
Uitto, J. [15 ]
Lifton, R. P. [1 ]
Paller, A. S. [16 ]
Milstone, L. M. [2 ]
Choate, K. A. [1 ,2 ,4 ]
机构
[1] Yale Univ, Dept Genet, Sch Med, POB 208059, New Haven, CT 06520 USA
[2] Yale Univ, Dept Dermatol, Sch Med, POB 208059, New Haven, CT 06520 USA
[3] Yale Univ, Dept Pediat, Sch Med, POB 208059, New Haven, CT 06520 USA
[4] Yale Univ, Dept Pathol, Sch Med, POB 208059, New Haven, CT 06520 USA
[5] Baylor Coll Med, Dept Dermatol, San Antonio, TX USA
[6] Univ Calif San Diego, Dept Dermatol, San Diego, CA 92103 USA
[7] Natl Skin Ctr, Dept Dermatol, Singapore, Singapore
[8] Childrens Hosp Los Angeles, Div Dermatol, Los Angeles, CA 90027 USA
[9] Childrens Hosp Los Angeles, Div Med Genet, Los Angeles, CA 90027 USA
[10] Complejo Hosp Univ, Dept Dermatol, Santiago De Compostela, Spain
[11] IDIS, CIBERER, Grp Med Xen USC, Fdn Publ Galega Med Xen SERGAS, Santiago De Compostela, Spain
[12] Complejo Hosp Univ Vigo, Serv Dermatol, Vigo, Spain
[13] Hosp Ninos Luis Calvo Mackenna, Dept Dermatol, Santiago, Chile
[14] Miller Sch Med, Dept Dermatol & Cutaneous Surg, Miami, FL USA
[15] Thomas Jefferson Univ, Dept Dermatol, Sidney Kimmel Med Coll, Philadelphia, PA 19107 USA
[16] Northwestern Univ, Dept Dermatol, Feinberg Sch Med, Chicago, IL 60611 USA
关键词
VARIANT;
D O I
10.1111/bjd.15570
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
引用
收藏
页码:319 / 322
页数:4
相关论文
共 50 条
  • [21] PNPLA1-Mediated Acylceramide Biosynthesis and Autosomal Recessive Congenital Ichthyosis
    Zeng, Fansi
    Qin, Wenzhen
    Huang, Feifei
    Chang, Pingan
    METABOLITES, 2022, 12 (08)
  • [22] Expanding the molecular and clinical spectrum of autosomal recessive congenital ichthyosis caused by pathogenic variants in NIPAL4 and PNPLA1 and evaluation of novel therapeutic interventions
    Rossel, S. V. J.
    Clabbers, J. M. K.
    Steijlen, P. M.
    van den Akker, P. C.
    Spuls, P. I.
    Middelkamp Hup, M. A.
    van Maarle, M. C.
    Vreeburg, M.
    Bolling, M. C.
    van Geel, M.
    Gostynski, A.
    JOURNAL OF THE EUROPEAN ACADEMY OF DERMATOLOGY AND VENEREOLOGY, 2023, 37 (12) : E1405 - E1409
  • [23] PNPLA1 defects in patients with autosomal recessive congenital ichthyosis and KO mice sustain PNPLA1 irreplaceable function in epidermal omega-O-acylceramide synthesis and skin permeability barrier
    Pichery, Melanie
    Huchenq, Anne
    Sandhoff, Roger
    Severino-Freire, Maella
    Zaafouri, Sarra
    Opalka, Lukas
    Levade, Thierry
    Soldan, Vanessa
    Bertrand-Michel, Justine
    Lhuillier, Emeline
    Serre, Guy
    Maruani, Annabel
    Mazereeuw-Hautier, Juliette
    Jonca, Nathalie
    HUMAN MOLECULAR GENETICS, 2017, 26 (10) : 1787 - 1800
  • [24] Autosomal Recessive Congenital Ichthyosis
    Rodriguez-Pazos, L.
    Ginarte, M.
    Vega, A.
    Toribio, J.
    ACTAS DERMO-SIFILIOGRAFICAS, 2013, 104 (04): : 270 - 284
  • [25] Autosomal Recessive Congenital Ichthyosis
    Fischer, Judith
    JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2009, 129 (06) : 1319 - 1321
  • [26] Autosomal recessive congenital ichthyosis: Genomic landscape and phenotypic spectrum in a cohort of 125 consanguineous families
    Youssefian, Leila
    Vahidnezhad, Hassan
    Saeidian, Amir Hossein
    Touati, Andrew
    Sotoudeh, Soheila
    Mahmoudi, Hamidreza
    Mansouri, Parvin
    Daneshpazhooh, Maryam
    Aghazadeh, Nessa
    Hesari, Kambiz Kamyab
    Basiri, Mohammadreza
    Londin, Eric
    Kumar, Gaurav
    Zeinali, Sirous
    Fortina, Paolo
    Uitto, Jouni
    HUMAN MUTATION, 2019, 40 (03) : 288 - 298
  • [27] Sixteen novel mutations in PNPLA1 in patients with autosomal recessive congenital ichthyosis reveal the importance of an extended patatin domain in PNPLA1 that is essential for proper human skin barrier function (vol 177, pg 445, 2017)
    Zimmer, A. D.
    Kim, G. -J.
    Hotz, A.
    Bourrat, E.
    Hausser, I
    Has, C.
    Oji, V
    Stieler, K.
    Vahlquist, A.
    Kunde, V
    Weber, B.
    Radner, F. P. W.
    Leclerc-Mercier, S.
    Schlipf, N.
    Demmer, P.
    Kusel, J.
    Fischer, J.
    BRITISH JOURNAL OF DERMATOLOGY, 2018, 178 (03) : 814 - 815
  • [28] PNPLA1 mutations cause recessive lamellar ichthyosis in humans and dogs: morphological correlations
    Hausser, I.
    Grall, A.
    Guaguere, E.
    Planchais, S.
    Grond, S.
    Bourrat, E.
    Hitte, C.
    Le Gallo, M.
    Derbois, C.
    Kim, G. J.
    Lagoutte, L.
    Degorce-Rubiales, F.
    Radner, F. P. W.
    Thomas, A.
    Kuery, C.
    Bensignor, E.
    Fontaine, J.
    Pin, D.
    Zimmermann, R.
    Zechner, R.
    Lathrop, M.
    Galibert, F.
    Andre, C.
    Fischer, J.
    EXPERIMENTAL DERMATOLOGY, 2012, 21 (09) : E3 - E3
  • [29] Impaired production of skin barrier lipid acylceramides and abnormal localization of PNPLA1 due to ichthyosis-causing mutations in PNPLA1
    Nohara, Tomohiro
    Ohno, Yusuke
    Kihara, Akio
    JOURNAL OF DERMATOLOGICAL SCIENCE, 2022, 107 (02) : 89 - 94
  • [30] Skin histopathology from patients with X-linked recessive ichthyosis and autosomal recessive congenital ichthyosis with transglutaminase 1 mutation
    Yang, C.
    Pomerantz, H.
    Corwin, J.
    Weinstock, M. A.
    Fleckman, P.
    DiGiovanna, J. J.
    Robinson-Bostom, L.
    JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2015, 135 : S34 - S34