Extreme Growth Failure is a Common Presentation of Ligase IV Deficiency

Jennie E. Murray, Louise S. Bicknell, Gökhan Yigit, Angela L. Duker, Margriet van Kogelenberg, Sara Haghayegh, Dagmar Wieczorek, Hülya Kayserili, Michael H. Albert, Carol A. Wise, January Brandon, Tjitske Kleefstra, Adilia Warris, Michiel van der Flier, J Steven Bamforth, Kurston Doonanco, Lesley Adès, Alan Ma, Michael Field, Diana JohnsonFiona Shackley, Helen Firth, C. Geoffrey Woods, Peter Nürnberg, Richard A. Gatti, Matthew Hurles, Michael B. Bober, Bernd Wollnik, Andrew P. Jackson

Research output: Contribution to journalArticlepeer-review

71 Citations (Scopus)
6 Downloads (Pure)


Ligase IV syndrome is a rare differential diagnosis for Nijmegen breakage syndrome owing to a shared predisposition to lympho-reticular malignancies, significant microcephaly, and radiation hypersensitivity. Only 16 cases with mutations in LIG4 have been described to date with phenotypes varying from malignancy in developmentally normal individuals, to severe combined immunodeficiency and early mortality. Here, we report the identification of biallelic truncating LIG4 mutations in 11 patients with microcephalic primordial dwarfism presenting with restricted prenatal growth and extreme postnatal global growth failure (average OFC -10.1 s.d., height -5.1 s.d.). Subsequently, most patients developed thrombocytopenia and leucopenia later in childhood and many were found to have previously unrecognized immunodeficiency following molecular diagnosis. None have yet developed malignancy, though all patients tested had cellular radiosensitivity. A genotype-phenotype correlation was also noted with position of truncating mutations corresponding to disease severity. This work extends the phenotypic spectrum associated with LIG4 mutations, establishing that extreme growth retardation with microcephaly is a common presentation of bilallelic truncating mutations. Such growth failure is therefore sufficient to consider a diagnosis of LIG4 deficiency and early recognition of such cases is important as bone marrow failure, immunodeficiency, and sometimes malignancy are long term sequelae of this disorder.

Original languageEnglish
Pages (from-to)76-85
Number of pages10
JournalHuman Mutation
Issue number1
Early online date8 Nov 2013
Publication statusPublished - Jan 2014

Bibliographical note

We thank Stephen Brown and Agnes Gallagher for technical support. A.P.J. is a MRC Senior Clinical Fellow and Lister Institute for Preventative MedicinePrize Fellow.
Disclosure statement: The authors declare no conflict of interest.

Funded by
Wellcome Trust. Grant Number: WT098051
Texas Scottish Rite Hospital for Children Research Fund
Potentials Foundation and Walking With Giants Foundation (WWGF)


  • ligase IV
  • LIG4
  • nonhomologous end joining
  • radiosensitivity
  • cytopenia
  • malignancy
  • DNA repair
  • immunodeficiency


Dive into the research topics of 'Extreme Growth Failure is a Common Presentation of Ligase IV Deficiency'. Together they form a unique fingerprint.

Cite this