Fontaine progeroid syndrome—A case report-Reference-Cited by-同舟云学术

Fontaine progeroid syndrome—A case report

Author:

Lally Sinéad¹^ORCID,Walsh Nicola²,Kenny Janna²,Franklin Orla³⁴,Cotter Melanie⁵⁶,Richardson Sarah⁷,McEligott Fiona⁸,Finan Alan¹

Affiliation:

1. Department of Paediatrics Cavan Monaghan Hospital, RCSI Hospital Group Cavan Ireland

2. Department of Clinical Genetics Children's Health Ireland at Crumlin Dublin 12 Ireland

3. Department of Paediatric Cardiology, Children's Health Ireland at Crumlin Dublin 12 Ireland

4. Department of Paediatric Cardiology Children's Health Ireland at Temple Street Dublin 1 Ireland

5. Department of Haematology Children's Health Ireland at Crumlin Dublin 12 Ireland

6. Department of Haematology Children's Health Ireland at Temple Street Dublin 1 Ireland

7. Department of Paediatrics Children's Health Ireland at Temple Street Dublin 1 Ireland

8. Department of Palliative Medicine Children's Health Ireland at Temple Street Dublin 1 Ireland

Publisher

Wiley

Subject

General Medicine

Link

Reference17 articles.

1. TillerGE.OMIM entry # 605104 RNA‐BINDING FOX1 HOMOLOG 1; RBFOX1.2000.

2. BocchiniCA.OMIM entry # 612289 FONTAINE PROGEROID SYNDROME; FPS.2018.

3. Lethal neonatal Hutchinson‐Gilford progeria syndrome;Rodríguez JI;J Med Genet,1999

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