Details

Autor(en) / Beteiligte

• Singh, Ram
• Cohen, Ana S A
• Poulton, Cathryn
• Hjortshøj, Tina Duelund
• Akahira-Azuma, Moe
• Mendiratta, Geetu
• Khan, Wahab A
• Azmanov, Dimitar N
• Woodward, Karen J
• Kirchhoff, Maria
• Shi, Lisong
• Edelmann, Lisa
• Baynam, Gareth
• Scott, Stuart A
• Jabs, Ethylin Wang

Titel

Deletion of ERF and CIC causes abnormal skull morphology and global developmental delay

Ist Teil von

• Cold Spring Harbor molecular case studies, 2021-06, Vol.7 (3), p.a005991

Ort / Verlag

United States: Cold Spring Harbor Laboratory Press

Erscheinungsjahr

2021

Quelle

MEDLINE

Beschreibungen/Notizen

• The ETS2 repressor factor (ERF) is a transcription factor in the RAS-MEK-ERK signal transduction cascade that regulates cell proliferation and differentiation, and pathogenic sequence variants in the gene cause variable craniosynostosis inherited in an autosomal dominant pattern. The reported variants are largely loss-of-function, implying haploinsufficiency as a primary disease mechanism; however, gene deletions have not been reported previously. Here we describe three probands with macrocephaly, craniofacial dysmorphology, and global developmental delay. Clinical genetic testing for fragile X and other relevant sequencing panels were negative; however, chromosomal microarray identified heterozygous deletions (63.7-583.2 kb) on Chromosome 19q13.2 in each proband that together included five genes associated with Mendelian diseases ( , , , , and ). Parental testing indicated that the aberrations were apparently de novo in two of the probands and were inherited in the one proband with the smallest deletion. Deletion of is consistent with the reported loss-of-function variants, prompting clinical copy-number-variant classifications of likely pathogenic. Moreover, the recent characterization of heterozygous loss-of-function sequence variants as a cause of intellectual disability and neurodevelopmental disorders inherited in an autosomal dominant pattern is also consistent with the developmental delays and intellectual disabilities identified among the two probands with deletions. Taken together, this case series adds to the previously reported patients with and/or sequence variants and supports haploinsufficiency of both genes as a mechanism for a variable syndromic cranial phenotype with developmental delays and intellectual disability inherited in an autosomal dominant pattern.