Skip to main content

A de novo 1.6Mb microdeletion at 19q13.2 in a boy with Diamond-Blackfan anemia, global developmental delay and multiple congenital anomalies



Microdeletions at 19q13.2 are very rare. Only two cases have been previously described. Here we report a 2-year-2-month old boy with Diamond-Blackfan anemia, global developmental delay, cognitive impairments, distinctive facial features, behavior problems, skeletal and genital dysplasia.

Case presentation

A de novo 1.6 Mb microdeletion at 19q13.2q13.31 was detected by chromosomal microarray analysis. Haploinsufficiency of the RPS19 gene is known to cause Diamond-Blackfan anemia, other features in this patient are likely due to the deletion of other candidate genes such as PAFAH1B3, ERF, LIPE and GSK3A.


The deletion detected in our patient overlapped and was significantly smaller than the ones previously reported, which offered the opportunity to further define the critical region for this proposed contiguous gene deletion syndrome.


Microdeletions at 19q13.2 have rarely been reported. Cario [1] and Tentler [2] each reported a case with microdeletion at 19q13.2 defined by FISH analysis respectively, thus the sizes and boundaries of the deletions were not precisely delineated. The clinical features of the two patients included Diamond Blackfan Anemia (DBA), global developmental delay, mental retardation, distinctive facial features and skeletal malformations [1, 2]. Haploinsufficiency of the RPS19 (OMIM 603474) gene involved in the deletions is known to cause DBA. DBA is a pure red-cell hypoplasia characterized by defective erythroid progenitor maturation and normal numbers and function of other haemopoietic cells [35]. It has been observed that patients with 19q13.2 microdeletion involving the RPS19 gene presented with a more complex clinical phenotype than those caused only by sequence variants in RPS19 gene [17]. Tentler et al. proposed that 19q13.2 deletion represented a novel contiguous gene deletion syndrome [2]. Here, we report a de novo 1.6 Mb microdeletion at 19q13.2q13.31 detected by chromosomal microarray in a 2-year-2-month old boy with many common features as reported in previous cases. The deletion detected in our patient was smaller and better defined by high resolution chromosomal microarray analysis. This case offered the opportunity for defining the critical region and discussing candidate genes associated with different phenotypes.

Case presentation

The proband was the first child of healthy unrelated parents and family history was unremarkable. Intrauterine growth retardation and oligohydramnios was noticed by ultrasound examination at 8 months of pregnancy. Because of progressive intrauterine growth retardation (IUGR), a delivery by cesarean section was performed at 37 weeks of gestation. Birth weight was 3.1 kg, length 47 cm (<−2SD) and head circumference 34 cm. Apgar scores were all 8. Feeding difficulty was noted at all times. At the age of 9 months he was referred to a pediatric clinic because of pallor. Hemoglobin concentration was 64 g/l and no reticulocytes were detected in peripheral blood. Bone marrow aspirate showed a selective decrease in erythroid precursors but otherwise normal cellularity. Hemoglobin concentration was recovered from 64 to 106 g/l after corticosteroid treatment.

The proband was 2 years 2 months old at the time of molecular evaluation. His weight was 9.9 kg (<−2SD), height 78 cm (<−3SD), and head circumference 47.5 cm, which indicated persistent failure to thrive. The developmental milestones were delayed: he raised his head at 7 months, sat alone at 1 year and could not independently walk yet. Language development was significantly delayed and he had almost complete absence of speech. He had moderate cognitive impairments. His distinctive facial features were characterized by cranial deformities, mild craniosynostosis, broad forehead, auricle dysplasia, arched and sparse eyebrows, hypertelorism, nystagmus and strabismus, broad nose with depressed nasal bridge, thick lips, teeth dysplasia, micrognathia, open-mouthed expression and drooling. He had skeletal abnormality including rib protrusion and kyphosis, but with normal level of calcium, phosphorus and alkaline phosphatase (Fig. 1). His abnormal behavior included mild self-mutilation, fingers biting, tongue stretching, anxiety and hyperactivity. He was insensitive to pain. Severe hypotonia and sleep disorders were present. Micropenis, small testes and anal fissure were detected. He had gastrointestinal dysfunction and suffered from frequent diarrhea. He would have high body temperature at night and return to normal at daylight spontaneously. Brain MRI, ultrasound and X-ray examinations for heart and lungs were all normal.

Fig. 1

The proband at 2-year-2-month age. Note cranial deformities, mild craniosynostosis, broad forehead, auricle dysplasia, hypertelorism, strabismus, broad nose with depressed nasal bridge, thick lips, micrognathia and open-mouthed expression, rib protrusion and kyphosis


Chromosome karyotype analysis

Cytogenetic investigations (GTG banding) on 20 metaphases obtained from PHA-stimulated peripheral lymphocytes of the patient were performed following standard protocols.

Chromosomal microarray analysis

Chromosomal microarray analysis was performed for the patient and both parents by Affymetrix Cytoscan HD Array (Affymetrix, USA). Genomic DNA was extracted from peripheral blood using a commercial kit (Qiagen). The labeling and hybridization procedures were performed following manufacturer’s instructions. The raw data of chromosomal microarray was analyzed by Affymetrix Chromosome Analysis Suite Software.

Confirmation of 19q13.2q13.31deletion

The deletion was further confirmed using quantitative real-time PCR analysis. Primer sequences and descriptions were included in Additional file 1: Table S1.


Standard chromosome analysis of peripheral blood by GTG banding was normal (data not shown). A 1.6 Mb microdeletion at 19q13.2q13.31 (chr19:42,306,042-43,906,653) was detected by chromosomal microarray analysis (Fig. 2). Parental chromosomal microarray analysis were normal. Thus, the proband carried a de novo copy number variant. The deletion was further confirmed by quantitative real-time PCR analysis (data not shown).

Fig. 2

Affymetrix cytoscan HD array analysis including weighted log2 ratio (upper), copy number state (middle) and allele peaks (lower) are shown for chromosome 19. The result shows microdeletion at 19q13.2q13.31. The genomic coordinates (hg19): chr19:42,306,042-43,906,653. The microdeletion region is denoted by a red bar

Discussion and conclusion

Microdeletions at 19q13.2 are very rare. So far, only two cases carrying a microdeletion at 19q13.2 have been reported who share similar clinical features including Diamond-Blackfan anemia, global developmental delay, skeletal abnormalities and intellectual disability. Both cases were detected by FISH analysis and the relative breakpoints and sizes estimation of the deletions were determined, whereas candidate genes except for RPS19 gene in this interval responsible for the complex clinical features of the patients were not identified [1, 2]. Our patient reported here carries a de novo 1.6 Mb microdeletion at 19q13.2q13.31 uncovered by high resolution chromosomal microarray analysis and no other clinical significant copy number variants are detected. The positions and sizes of three cases are delineated in Fig. 3. The clinical presentations in all three cases are summarized in Table 1.

Fig. 3

Top panel shows a genome view of all deletion cases (red colored custom tracks) relative to the genomic coordinates at 19q13.2q13.31 region, extracted from Human Genome Build 37 (hg19). Blue block diagram represents critical region of 19q13.2. Bottom panel shows the zoomed-in 19q13.2 critical region encompassing candidate genes

Table 1 Clinical features observed in patients with 19q13.2 deletion

Haploinsufficiency of the RPS19 gene is responsible for the Diamond-Blackfan anemia phenotype in these patients. RPS19 deletion is not likely to cause other features observed in these individuals since none of the patients with DBA caused by RPS19 gene point mutations has developmental delay, intellectual disability or dysmorphism features [57]. Furthermore, a girl reported to carry a de novo balanced translocation t(X;19) (p21;q13) which interrupted the RPS19 gene also had normal development without skeletal malformations [3, 4]. These findings further suggested that other genes at 19q13.2 locus contributed to other clinical features observed in these patients.

Based on this notion, we analyzed all genes involved in the deleted interval detected in our patient in Additional file 2: Table S2. And we identified several candidate genes that could explain the additional features seen in our patient. The PAFAH1B3 (OMIM 603074) gene maps in 19q13.2 region. Mutations or deletions of PAFAH1B1 gene result in Miller-Dieker syndrome characterized by lissencephaly, severe intellectual disability, developmental delay, distinctive facial features, seizures, hypotonia and feeding difficulties. PAFAH1B1 is a subunit of a brain platelet-activating factor acetylhydrolase (PAFAH1B) where it forms a heterotrimeric complex with two hydrolase subunits, referred to as 29 kDa (PAFAH1B3) and 30 kDa (PAFAH1B2). In the brain, PAFAH1B complex regulates the level of platelet activating factor, which is thought to be involved in neuronal migration essential for normal brain development and function [810].

Haploinsufficiency of ERF (OMIM 611888) gene involved in this interval leads to complex craniosynostosis recognized by multiple-suture synostosis, craniofacial dysmorphism, Chiari malformation, behavior problems and language delay [11, 12].

Among other genes in this interval, we identified the LIPE (OMIM 151750) and GSK3A (OMIM 606784) as candidate genes. Animal model shows that hormone sensitive lipase encoded by LIPE gene is a multifunctional fatty acyl esterase that causes male infertility and decreased testes weight and also plays an important role in the function of adipocytes, pancreatic-cells, and adrenal cortical cells [1315]. Glycogen synthase kinase 3 (GSK3), encoded by GSK3A and GSK3B genes, is shown to be expressed ubiquitously in all mammalian tissues and is also essential for normal sperm function required for male fertility [16, 17]. Furthermore GSK3 is implicated to be associated with a variety of diseases including mood disorders, Alzheimer disease, diabetes and cancer, and plays a role in embryo development as well [1719]. Taken together, these candidate genes involved in 19q13.2 region could explain the complex clinical phenotype observed in our patient.

In conclusion, we report a de novo microdeletion at 19q13.2q13.31 in a patient with DBA, global developmental delay, cognitive impairments, facial dysmorphism, behavior problems, skeletal and genital dysplasia. Our patient exhibited strikingly similar clinical phenotypes among those patients with 19q13.2 microdeletions. Haploinsufficiency of the RPS19 is the cause of DBA and several candidate genes responsible for other clinical features are identified in this interval, which further suggests a novel contiguous gene deletion syndrome and the critical region at 19q13.2 locus is defined as well.


DBA Diamond Blackfan Anaemia; GSK3 glycogen synthase kinase 3; IUGR intrauterine growth retardation


  1. 1.

    Cario H, Bode H, Gustavsson P, Dahl N, Kohne E. A microdeletion syndrome due to a 3-Mb deletion on 19q13.2--Diamond-Blackfan anemia associated with macrocephaly, hypotonia, and psychomotor retardation. Clin Genet. 1999;55(6):487–92.

    CAS  Article  PubMed  Google Scholar 

  2. 2.

    Tentler D, Gustavsson P, Elinder G, Eklöf O, Gordon L, Mandel A, et al. A microdeletion in 19q13.2 associated with mental retardation, skeletal malformations, and Diamond-Blackfan anaemia suggests a novel contiguous gene syndrome. J Med Genet. 2000;37(2):128–31.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  3. 3.

    Gustavsson P, Skeppner G, Johansson B, Berg T, Gordon L, Kreuger A, et al. Diamond-Blackfan anaemia in a girl with a de novo balanced reciprocal X;19 translocation. J Med Genet. 1997;34(9):779–82.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  4. 4.

    Gustavsson P, Willing TN, van Haeringen A, Tchernia G, Dianzani I, Donnér M, et al. Diamond-Blackfan anaemia: genetic homogeneity for a gene on chromosome 19q13 restricted to 1.8 Mb. Nat Genet. 1997;16(4):368–71.

    CAS  Article  PubMed  Google Scholar 

  5. 5.

    Gustavsson P, Garelli E, Draptchinskaia N, Ball S, Willig TN, Tentler D, et al. Identification of microdeletions spanning the Diamond-Blackfan anemia (DBA) locus on 19q13 and evidence for genetic heterogeneity. Am J Hum Genet. 1998;63(5):1388–95.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  6. 6.

    Draptchinskaia N, Gustavsson P, Andersson B, Pettersson M, Willig TN, Dianzani I, et al. The gene encoding ribosomal protein S19 is mutated in Diamond-Blackfan anaemia. Nat Genet. 1999;21(2):169–75.

    CAS  Article  PubMed  Google Scholar 

  7. 7.

    Dianzani I, Garelli E, Ramenghi U. Diamond-Blackfan Anaemia: an overview. Paediatr Drugs. 2000;2(5):345–55.

    CAS  Article  PubMed  Google Scholar 

  8. 8.

    Sweeney KJ, Clark GD, Prokscha A, Dobyns WB, Eichele G. Lissencephaly associated mutations suggest a requirement for the PAFAH1B heterotrimeric complex in brain development. Mech Dev. 2000;92(2):263–71.

    CAS  Article  PubMed  Google Scholar 

  9. 9.

    Escamez T, Bahamonde O, Tabares-Seisdedos R, Vieta E, Martinez S, Echevarria D. Developmental dynamics of PAFAH1B subunits during mouse brain development. J Comp Neurol. 2012;520(17):3877–94.

    Article  PubMed  Google Scholar 

  10. 10.

    Iglesias Escalera G, Carrasco Marina ML, Martín Del Valle F, Martínez Guardia N, Rodríguez L, Martínez-Fernández ML. Miller-Dieker syndrome. An Pediatr (Barc). 2009;70(3):304–6.

    CAS  Article  Google Scholar 

  11. 11.

    Chaudhry A, Sabatini P, Han L, Ray PN, Forrest C, Bowdin S. Heterozygous mutations in ERF cause syndromic craniosynostosis with multiple suture involvement. Am J Med Genet A. 2015;167A(11):2544–7. doi:10.1002/ajmg.a.37218.

    Article  PubMed  Google Scholar 

  12. 12.

    Twigg SR, Vorgia E, McGowan SJ, Peraki I, Fenwick AL, Sharma VP, et al. Reduced dosage of ERF causes complex craniosynostosis in humans and mice and links ERK1/2 signaling to regulation of osteogenesis. Nat Genet. 2013;45(3):308–13.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  13. 13.

    Wang SP, Chung S, Soni K, Bourdages H, Hermo L, Trasler J, et al. Expression of human hormone-sensitive lipase (HSL) in postmeiotic germ cells confers normal fertility to HSL-deficient mice. Endocrinology. 2004;145(12):5688–93.

    CAS  Article  PubMed  Google Scholar 

  14. 14.

    Wang SP, Wu JW, Bourdages H, Lefebvre JF, Casavant S, Leavitt BR, et al. The catalytic function of hormone-sensitive lipase is essential for fertility in male mice. Endocrinology. 2014;155(8):3047–53.

    Article  PubMed  Google Scholar 

  15. 15.

    Chung S, Wang SP, Pan L, Mitchell G, Trasler J, Hermo L. Infertility and testicular defects in hormone-sensitive lipase-deficient mice. Endocrinology. 2001;142(10):4272–81.

    CAS  Article  PubMed  Google Scholar 

  16. 16.

    Kaidanovich-Beilin O, Woodgett JR. GSK-3: functional insights from cell biology and animal models. Front Mol Neurosci. 2011;4:40. doi:10.3389/fnmol.2011.00040.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  17. 17.

    Medina M, Wandosell F. Deconstructing GSK-3: the fine regulation of its activity. Int J Alzheimers Dis. 2011;2011:479249. doi:10.4061/2011/479249.

    PubMed  PubMed Central  Google Scholar 

  18. 18.

    Bhattacharjee R, Goswami S, Dudiki T, Popkie AP, Phiel CJ, Kline D, et al. Targeted disruption of glycogen synthase kinase 3A (GSK3A) in mice affects sperm motility resulting in male infertility. Biol Reprod. 2015;92(3):65. doi:10.1095/biolreprod.114.124495.

    Article  PubMed  PubMed Central  Google Scholar 

  19. 19.

    Aparicio IM, Garcia-Herreros M, Fair T, Lonergan P. Identification and regulation of glycogen synthase kinase-3 during bovine embryo development. Reproduction. 2010;140(1):83–92.

    CAS  Article  PubMed  Google Scholar 

Download references


We would like to thank the family of the proband for their cooperation with this study.


Not applicable.

Availability of data and materials

Affymetrix Cytoscan HD (

Affymetrix Chromosome Analysis Suite Software (

Authors’ contributions

HY carried out the cytogenetic studies and wrote the manuscript. LL made the clinical evaluation and collected clinical information of the patient in detail. Others coordinated the clinical evaluation. All the authors have read and approved the manuscript.

Competing interests

The authors declare that they have no competing interest.

Consent for publication

Written informed consent was obtained from the patient for publication of this case report and any accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of this journal.

Author information



Corresponding author

Correspondence to Liyang Liang.

Additional files

Additional file 1: Table S1.

Primers information. (DOCX 23 kb)

Additional file 2: Table S2.

All genes in the deleted interval detected in our patient. (DOCX 19 kb)

Rights and permissions

Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (, which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( applies to the data made available in this article, unless otherwise stated.

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

Yuan, H., Meng, Z., Liu, L. et al. A de novo 1.6Mb microdeletion at 19q13.2 in a boy with Diamond-Blackfan anemia, global developmental delay and multiple congenital anomalies. Mol Cytogenet 9, 58 (2016).

Download citation


  • Microdeletion
  • 19q13.2
  • Diamond-Blackfan Anemia
  • Global developmental delay
  • Cognitive impairments
  • Behavior problems