O'Donnel-Luria-Rodan (ODLURO) syndrome is a neurodevelopmental disorder with autosomal dominant inheritance. It appears more frequently in males during the first decade of life and is associated with developmental delay, low intelligence quotient, autism spectrum disorder-like behavior, epilepsy, speech delay, aggression, facial and skeletal deformities, gastrointestinal symptoms and hypotonia. Although few cases have been documented, it appears that the phenotype spectrum may vary, especially between the two biological sexes. The present study reported a case of a 5-year-old male patient who was diagnosed with ODLURO at the age of 4 years using whole-exome sequencing. Molecular analysis identified a new mutation in the lysine methyltransferase 2E (inactive) (KMT2E) gene, which was classified as a variant with unknown significance. The father, who presented with non-specific and undiagnosed psychiatric manifestations, presented the same KMT2E variant. The case described in the present study is not only interesting because there are <40 cases described in the literature, but also because a new inherited mutation in the KMT2E gene, present in both father and son, that resulted in different phenotypic manifestations was identified.
O'Donnel-Luria-Rodan (ODLURO) syndrome was first reported in 2019 in 30 patients, with the majority of patients being under the age of 10 years. To date, there have been 38 reported cases worldwide (
The lysine methyltransferase 2E (inactive) (KMT2E) gene encodes a member of the lysine N-methyltransferase-2 family, a group of enzymes that serve an important role in chromatin remodeling through transcriptional regulation. ODLURO is caused by mutations in the KMT2E gene that result in pathogenic enzyme variants responsible for regulating histone 4 methylation on lysine 3 (H3K4). Lack of proper methylation leads to abnormalities in the molecular activity of neurons. As methylation maintains the open chromatin state, any dysregulation affects proper transcription regulation. H3K4 methylation undergoes dynamic changes during the neurodevelopmental phase, impacting both the environment of neural and glial cells in the brain and the molecular activity of the neurons (
O'Donnell-Luria identified 31 different mutations in the heterozygous state for the KMT2E gene in a group of 34 individuals with ODLURO syndrome (OMIM 618512) (
The present study reports the case of a 5-year-old male patient diagnosed with ODLURO syndrome at the age of 4 years, who was the first reported patient with ODLURO in Romania. The patient was the only child of non-consanguineous parents and the family history was negative. The patient was born at term after an uncomplicated pregnancy and delivery, and displayed normal parameters at birth.
Gross motor development was delayed, as the patient began sitting at 7 months and walking at 15 months of age. Verbal skill communication was never acquired and the mother noticed behavioral anomalies, including avoidance of gaze, retreating into repetitive, self-centered games, and no interaction with other children of his age. After the age of 2 years, the patient was consulted by several pediatric neurologists and psychiatrists, but in the absence of specific magnetic resonance imaging anatomical and electrophysiological functional abnormalities of the CNS, the patient was diagnosed with an idiopathic autistic spectrum disorder. At the age of 5 years, the patient was referred for medical genetic assessment. Overall development showed the-standard deviation values of height and weight for the age. The patient recognized only a few basic, short words, but could not reproduce them or verbally communicate in any way. The patient's father also faced challenges with social interactions, living isolated from the family and displaying autistic behaviors, but had not undergone a psychological evaluation.
Intellectual disability was objectified by the psychologist using specific evaluation tools, and the patient presented with an IQ of 52. The patient also displayed the following characteristics: Self-isolation, repetitive and unusual body movements, paroxysmal crying, reduced attention span to 6-7 sec and difficulty making eye contact. All of these, in addition with the presentations of anxiety and a tendency to self-harm indicated an autism spectrum disorder.
The patient had light, sensitive skin, blonde hair, blue eyes, and presented macrocephaly and mild facial dysmorphia, including antimongoloid slanting palpebral fissures, prominent nasolabial folds and frontal bossing. Another interesting finding was the narrowing of the distal phalanx of the patient's fingers (
Among the most debilitating symptoms, severe gastroesophageal reflux with recurrent nausea, vomiting and abdominal pain was reported. Nutrigenomic testing was recommended, and the results revealed a tendency for compulsive eating behaviors, especially for calorie-rich foods. Moreover, the specific HLA DQ 2.5 haplotype defines a predisposition to developing celiac disease due to gluten intolerance.
Due to the heterogeneous, non-specific clinical manifestations, whole-exome sequencing (WES) was performed with parental informed consent. The investigator reported a heterozygous mutation in the KMT2E gene (KMT2E NM_018682.3: c.498-11T>C), which was characterized by a deletion that resulted in the inclusion of a pathogenic exon in the mature mRNA, thus altering the structure and function of the synthesized polypeptide. Targeted genetic testing was performed in both parents, and the variant was identified in the father (
ODLURO is a newly defined genetic condition, and as with most rare genetic diseases, there is little information in the literature on its etiopathogenesis. The authors who defined this syndrome revealed an association between KMT2E gene mutations and a clinical phenotype with several common elements, including neurodevelopmental delay with autistic behavior and intellectual disability, non-specific facial dysmorphia and various functional abnormalities (
The patient reported in the present study was a 5-year-old male who was diagnosed with ODLURO based on clinical manifestations and a heterozygous mutation in the KMT2E gene (KMT2E NM_018682.3: c.498-11T>C), which is currently classified as a variant of uncertain significance (VUS) due to the lack of reported cases with this genetic variant in the medical literature related to ODLURO. The same variant was identified in the patient's father, who also presented with psychiatric symptoms, but not to the same severity as the patient. In this case, VUS management and evaluating a possible etiopatogenic link with the phenotype was challenging. The label VUS emerges if no reports connect the variant to the specific disease. Also, if a variant is extremely rare, it might take time to conduct comprehensive studies and catalog enough cases that associate it with a medical condition. The arguments that the identified variant may be pathogenic are due to its molecular characteristics; According to the investigator,
Although the majority of cases of ODLURO are a consequence of a de novo mutation, inheritance was identified in a family with three affected siblings (
Autism spectrum disorder is common in patients with ODLURO, especially in males, together with speech delay, intellectual disability, anxiety and aggressive behavior (
Facial dysmorphic features like dolichocephaly, large forehead, deep-set eyes, antimongoloid palpebral fissures, periorbital fullness, prominent cheeks and prominent nasolabial folds have been described in patients with ODLURO (
Gastrointestinal symptoms have also been reported in numerous patients with ODLURO (
In conclusion, based on the aforementioned genetic findings and taking into consideration the phenotype of the patient, the c.498-11T>C, KMT2E VUS was a potential cause for the patient's symptoms. However, further studies are required to confirm the pathogenicity of the variant. It appeared that the mutation was inherited from the father and decreased penetrance may explain the milder phenotype, restricted to autistic-like behavior, therefore further functional and clinical studies are necessary and will allow precise pinpointing of the pathologic significance of this variant. The case reported in the present study is an example of rare disease challenges for diagnostic uncertainty when considering the unknown clinical significance of a specific variant. Until further evidence for the identified variant has been identified, the case reported in the present study should remain in focus as the first case of ODLURO diagnosed in Romania.
ODLURO is a rare neurodevelopmental disorder caused by a germline mutation in the KMT2E gene that is primarily
Not applicable.
The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.
AC and MSM conducted the genetic consult and counselling. AC, ZCB, EK, DM and II interpreted the genetic test results and confirmed the authenticity of all the raw data. All authors read and approved the final manuscript.
Not applicable.
The patient's family provided consent for publication.
The authors declare that they have no competing interests.
Facial phenotype and tapering fingers. (A and C) Facial phenotype of the patient with dolichocephaly, prominent forehead and antimongoloid palpebral fissures. (B) Tapering fingers of the patient.
Clinical features of the presented patient in comparison with other reported patients with ODLURO syndrome (
Clinical features in ODLURO syndrome | Manifestations in previously reported cases | Manifestations in the presented case |
---|---|---|
Facial dysmorphic features | Dolichocephaly, large forehead, deep-set eyes, antimongoloid palpebral fissures, periorbital fullness, prominent cheeks and prominent nasolabial folds | Macrocephaly, frontal bossing, antimongoloid palpebral fissures, prominent cheeks and prominent nasolabial folds |
Height, weight, and developmental abnormalities | Short stature and delayed development | Delayed physical development |
Osteoarticular abnormalities | Tapering fingers | Tapering fingers |
Neurological and psychiatric involvement | Hypotonia, seizures, intellectual disability, delayed speech, anxiety and autism | Autism, intellectual disability, lack of verbal communication, anxiety and eating disorders |
Cardiovascular involvement | Septal defects | N/A |
Gastroenterological involvement | Nausea, vomiting, motility disorder and gastroesophageal reflux | Nausea, vomiting, motility disorder and gastroesophageal reflux |
Immunological involvement | N/A | Positive for HLA DQ 2.5, which results in a predisposition to developing celiac disease |
ODLURO, O'Donnel-Luria-Rodan.