Literature DB >> 14726869

Infantile systemic hyalinosis.

Helen T Shin1, Amy Paller, George Hoganson, Judith P Willner, Mary Wu Chang, Seth J Orlow.   

Abstract

Infantile systemic hyaloinosis is a rare, progressive, and fatal disease that is inherited in an autosomal recessive fashion. We describe 2 patients in whom thickened skin; small nodules of the perianal region, face, and neck; joint contractures; growth failure; diarrhea; and frequent infections developed within the first few weeks of life. Both patients died before 2 years of age.

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Mesh:

Year:  2004        PMID: 14726869     DOI: 10.1016/s0190-9622(03)02798-1

Source DB:  PubMed          Journal:  J Am Acad Dermatol        ISSN: 0190-9622            Impact factor:   11.527


  12 in total

1.  Case report: Infantile systemic hyalinosis: a dental perspective.

Authors:  D Olczak-Kowalczyk; E Krasuska-Slawinska; D Rokicki; M Pronicki
Journal:  Eur Arch Paediatr Dent       Date:  2011-08

2.  Infantile Systemic Hyalinosis: A Case Report of Compromised Cellular and Humoral Branches of the Immune System Leading to Infections.

Authors:  Yana Klebanova; Christina Schwindt
Journal:  Pediatr Asthma Allergy Immunol       Date:  2009-09

3.  Infantile systemic hyalinosis: a case report with a novel mutation.

Authors:  Siham Al Sinani; Fathyia Al Murshedy; Reem Abdwani
Journal:  Oman Med J       Date:  2013-01

Review 4.  Infantile systemic hyalinosis presenting as intractable infantile diarrhea.

Authors:  Luluah Al-Mubarak; Abdulkarim Al-Makadma; Sultan Al-Khenaizan
Journal:  Eur J Pediatr       Date:  2008-06-18       Impact factor: 3.183

5.  Infantile systemic hyalinosis: Report of two severe cases from Saudi Arabia and review of the literature.

Authors:  Sahar Ahmed Fathi Hammoudah; Lama Mohammed El-Attar
Journal:  Intractable Rare Dis Res       Date:  2016-05

6.  Juvenile Hyaline Fibromatosis- A Rare Autosomal Recessive Disease.

Authors:  Prarthana Sameer Kalgaonkar; Minal Wade; Charusheela Warke; Meena Makhecha; Manisha Khare
Journal:  J Clin Diagn Res       Date:  2017-07-01

7.  Infantile systemic hyalinosis: A case report and review of literature.

Authors:  Bhushan Madke; Vidya Kharkar; Sunanda Mahajan; Siddhi Chikhalkar; Uday Khopkar
Journal:  Indian Dermatol Online J       Date:  2010-07

8.  Infantile Systemic Hyalinosis: Report of 17-year Experience.

Authors:  Seyed Reza Raeeskarami; Yahya Aghighi; Azadeh Afshin; Abdolreza Malek; Ali Zamani; Vahid Ziaee
Journal:  Iran J Pediatr       Date:  2014-12-09       Impact factor: 0.364

9.  Protein-losing enteropathy and joint contractures caused by a novel homozygous ANTXR2 mutation.

Authors:  Edith Schussler; Rita V Linkner; Jacob Levitt; Lakshmi Mehta; John A Martignetti; Kimihiko Oishi
Journal:  Adv Genomics Genet       Date:  2018-06-27

10.  Clinical aspects of Hyaline Fibromatosis Syndrome and identification of a novel mutation.

Authors:  Bettina Härter; Francesco Benedicenti; Daniela Karall; Ekkehard Lausch; Gisela Schweigmann; Franco Stanzial; Andrea Superti-Furga; Sabine Scholl-Bürgi
Journal:  Mol Genet Genomic Med       Date:  2020-03-20       Impact factor: 2.183

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