Literature DB >> 21165217

Multiple epidermal cysts in lowe syndrome.

Jong Hoon Won1, Min Jung Lee, Joon Soo Park, Hyun Chung, Jin Kyung Kim, Jeong Su Shim.   

Abstract

Lowe syndrome is a rare genetic disease that appears to cause various clinical symptoms involving the eye, nervous system, and kidney. While a mutation of the OCRL1 gene is known to be responsible for this syndrome, the exact pathophysiology remains unclear. Various multi-organ symptoms are characteristic of Lowe syndrome, but skin lesions have rarely been described. Recently, mechanisms for the association of Lowe syndrome and skin lesions have been proposed. We report this case of Lowe syndrome involving multiple epidermal cysts on the scalp in a 6-year-old male child.

Entities:  

Keywords:  Epidermal cyst; Lowe syndrome

Year:  2010        PMID: 21165217      PMCID: PMC2991724          DOI: 10.5021/ad.2010.22.4.444

Source DB:  PubMed          Journal:  Ann Dermatol        ISSN: 1013-9087            Impact factor:   1.444


  10 in total

1.  Lowe syndrome: case report.

Authors:  Y Batirbaygil; M Turgut
Journal:  J Clin Pediatr Dent       Date:  1999       Impact factor: 1.065

2.  Organic-aciduria, decreased renal ammonia production, hydrophthalmos, and mental retardation; a clinical entity.

Authors:  C U LOWE; M TERREY; E A MacLACHLAN
Journal:  AMA Am J Dis Child       Date:  1952-02

3.  The effect of missense mutations in the RhoGAP-homology domain on ocrl1 function.

Authors:  U Lichter-Konecki; L W Farber; J S Cronin; S F Suchy; R L Nussbaum
Journal:  Mol Genet Metab       Date:  2006-06-13       Impact factor: 4.797

4.  Glaucoma with the oculocerebrorenal syndrome of Lowe.

Authors:  David S Walton; Garyfallia Katsavounidou; Charles U Lowe
Journal:  J Glaucoma       Date:  2005-06       Impact factor: 2.503

5.  Renal manifestations of Dent disease and Lowe syndrome.

Authors:  Hee Yeon Cho; Bum Hee Lee; Hyun Jin Choi; Il Soo Ha; Yong Choi; Hae Il Cheong
Journal:  Pediatr Nephrol       Date:  2007-11-24       Impact factor: 3.714

6.  Eruptive vellus hair cysts in a patient with Lowe syndrome.

Authors:  Maithily A Nandedkar; Harold Minus; Meenakshi A Nandedkar
Journal:  Pediatr Dermatol       Date:  2004 Jan-Feb       Impact factor: 1.588

7.  Lowe oculocerebrorenal syndrome in a female with a balanced X;20 translocation: mapping of the X chromosome breakpoint.

Authors:  O T Mueller; J K Hartsfield; L A Gallardo; Y P Essig; K L Miller; P R Papenhausen; T A Tedesco
Journal:  Am J Hum Genet       Date:  1991-10       Impact factor: 11.025

8.  Different seizure types and skin lesions in oculocerebrorenal syndrome of Lowe.

Authors:  Füsun Erdogan; Sevda Ismailogullari; Isin Soyuer; Ayten Ferahbas; Hakan Poyrazoglu
Journal:  J Child Neurol       Date:  2007-04       Impact factor: 1.987

9.  Lowe syndrome, a deficiency of phosphatidylinositol 4,5-bisphosphate 5-phosphatase in the Golgi apparatus.

Authors:  S F Suchy; I M Olivos-Glander; R L Nussabaum
Journal:  Hum Mol Genet       Date:  1995-12       Impact factor: 6.150

Review 10.  Lowe syndrome.

Authors:  Mario Loi
Journal:  Orphanet J Rare Dis       Date:  2006-05-18       Impact factor: 4.123

  10 in total
  2 in total

Review 1.  The oculocerebrorenal syndrome of Lowe: an update.

Authors:  Arend Bökenkamp; Michael Ludwig
Journal:  Pediatr Nephrol       Date:  2016-03-24       Impact factor: 3.714

2.  Lowe syndrome: a single center's experience in Korea.

Authors:  Hyun-Kyung Kim; Ja Hye Kim; Yoo-Mi Kim; Gu-Hwan Kim; Beom Hee Lee; Jin-Ho Choi; Han-Wook Yoo
Journal:  Korean J Pediatr       Date:  2014-03-31
  2 in total

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