Subject(s)
Orofaciodigital Syndromes , Humans , Orofaciodigital Syndromes/diagnosis , Male , Female , Magnetic Resonance ImagingABSTRACT
A hamartoma is a benign proliferation of typical mature cells specific to a particular anatomical site. In the oral cavity, they may occur as isolated cases or be associated with genetic syndromes. Oral-facial-digital syndrome type VI is a rare genetic disorder with an estimated incidence of one in 50,000-250,000 newborns. Here, we report a case of a 2-year-old boy diagnosed with oral-facial-digital syndrome type VI who was referred for evaluation of a bilateral and normochromic to slightly pinkish nodule on the lateral surface of the tongue. Clinically, the child presented hypotonia, low visual acuity, absence of oculocephalic reflex, delay in neuropsychomotor development, and polydactyly in the feet. Excisional biopsies of both sides of the tongue were performed using a 1.5 W high-power diode laser (wavelength of 980 nm), and histopathological analysis revealed abundant mature adipocytes predominantly arranged in lobules that mainly surrounded the minor salivary gland parenchyma. The surgical sites healed with no complications and the patient remains under follow-up for 10 months. Due to the limited literature on this syndrome and the frequent presence of tongue hamartomas in children, dentists need to be familiar with them.
Subject(s)
Hamartoma , Orofaciodigital Syndromes , Tongue Diseases , Humans , Hamartoma/pathology , Male , Orofaciodigital Syndromes/pathology , Orofaciodigital Syndromes/diagnosis , Child, Preschool , Tongue Diseases/pathology , Tongue Diseases/diagnosis , BiopsyABSTRACT
BACKGROUND: Oro-facial digital(OFD) syndrome is a rare anomaly which is often missed out as just cleft lip and palate.It is an X-linked dominant condition with lethality in males. It however results from the pleotropic effect of a morphogenetic impairment affecting almost invariably the mouth, face and digits and it also includes lower IQ and mental retardation. 14 different variations of these syndrome can be seen with the majority of cases of type 1 and 2 based on characteristic clinical manifestations. CASE REPORT: Present case report describes a 9 year old girl patient who was mis-diagnosed with partial cleft palate and was later diagnosed as orofacial digital syndrome based on the clinical and oral features. CONCLUSION: Not much literature is present regarding this topic and with no relevent family history makes this case a one in a million case of OFD. Therefore, this case report is a complete insight on Oro-facial digital syndrome.
Subject(s)
Cleft Lip , Cleft Palate , Mouth Abnormalities , Orofaciodigital Syndromes , Male , Female , Humans , Child , Cleft Palate/diagnosis , Orofaciodigital Syndromes/diagnosis , FaceSubject(s)
Orofaciodigital Syndromes , Polycystic Kidney Diseases , Polycystic Kidney, Autosomal Dominant , Humans , Polycystic Kidney, Autosomal Dominant/complications , Polycystic Kidney, Autosomal Dominant/diagnosis , Polycystic Kidney, Autosomal Dominant/genetics , Orofaciodigital Syndromes/diagnosis , Orofaciodigital Syndromes/genetics , Polycystic Kidney Diseases/diagnosis , Polycystic Kidney Diseases/genetics , KidneyABSTRACT
Orofaciodigital syndrome type 1 (OFDS1) is a genetic disorder characterized by specific oral, facial, and limb malformations. A 14-month-old girl with congenital cleft palate, lower lip midline cleft, and digital anomalies admitted to our hospital was preliminarily diagnosed with OFDS1. Genetic analysis revealed that she carried a heterozygous variant of OFD1 at locus Xp22.2 on the X chromosome. Herein, we present the specific phenotype and genotype and the treatment modalities for this patient and references for diagnosing and treating OFDS.
Subject(s)
Cleft Palate , Limb Deformities, Congenital , Orofaciodigital Syndromes , Female , Humans , Orofaciodigital Syndromes/diagnosis , Orofaciodigital Syndromes/genetics , Exons , Face , Cleft Palate/diagnosis , Cleft Palate/genetics , Cleft Palate/surgeryABSTRACT
Oral-facial-digital syndrome (OFDS) is a multisystemic ciliopathic disorder with an autosomal recessive mode of inheritance. OFDS usually manifests with typical craniofacial anomalies and variable occurrence of polydactyly. Germline variants in CPLANE1 cause OFDS VI. In this study, we investigated a 26-year-old Chinese female patient who was 23+1 weeks pregnant. She had a history of adverse pregnancy outcomes with multiple foetal malformations. We performed ultrasonography and identified the foetus as having a posterior fossa Blake cyst and postaxial polydactyly. The patient decided to terminate her pregnancy, and further genetic molecular analysis was performed. We identified the aborted foetus as having postaxial polydactyly. Whole-exome sequencing identified a missense variant (c.3599C>T, p.A1200V) in exon 20 and a c.834+1G>T variant in exon 7 of CPLANE1 (NM_023073.3) in the foetus. Sanger sequencing confirmed that these variants came from the parents of the foetus. In this study, we investigated a family with OFDS VI through genetic testing and bioinformatics analysis, which provided powerful help for prenatal diagnosis. Then, we demonstrated that the cell migration rate and the number of cilia were decreased after interference with CPLANE1 expression in NIH/3T3 cells. After CPLANE1 knockdown, the Hh signalling pathway was inhibited, and the Hh pathway activator SAG reversed the inhibitory effect. This is the first report of a family with OFDS VI in the Chinese population.
Subject(s)
Abnormalities, Multiple , Orofaciodigital Syndromes , Polydactyly , Abnormalities, Multiple/genetics , Adult , Animals , Cilia/genetics , Female , Fingers/abnormalities , Humans , Mice , Orofaciodigital Syndromes/diagnosis , Orofaciodigital Syndromes/genetics , Pregnancy , Toes/abnormalities , Exome SequencingABSTRACT
Oral-facial digital (OFD) syndrome is characterized by abnormalities of the face (hypertelorism and low set-ears), oral cavity (multiple frenula, lingual hamartoma, or lobulated tongue) and extremities (postaxial polydactyly). At least 19 genes have been implicated in the development of OFD syndrome. Herein, we report the case a 13-year-old patient with atrioventricular septal defect, moderate intellectual disability, epilepsy, and features of OFD, including multiple oral frenula, and postaxial polydactyly of the hands and feet. The patient had a de novo heterozygous variant in PRKACB: chr1(GRCh37):g.84700915T > C, c.1124T > C (NM_182948.4), p.(Phe375Ser). To date, four patients with pathogenic monoallelic variants in PRKACB have been reported, and the condition associated with these variants is referred to as Cardioacrofacial dysplasia-2 (CAFD2, MIM619143). Previously reported features of this condition include congenital heart disease (e.g., atrioventricular septal defect) and postaxial polydactyly, and two of the patients had multiple oral frenula. We suggest that a significant phenotypic overlap exists between CAFD2 and OFD syndrome, in that these patients especially share the features of postaxial polydactyly and multiple oral frenula. The phenotypic similarity between patients with CAFD2 and classic OFD syndrome with an OFD1 variant might be explained by the recent in vitro experimental finding that a protein kinase A subunit encoded by PRKACB directly phosphorylates the OFD1 protein. From the standpoint of genetic counseling, OFD syndrome type1, the prototypic form of OFD, exhibits an X-linked dominant inheritance pattern, whereas other forms of OFD syndrome exhibit an autosomal recessive inheritance pattern. Recognition of CAFD2 as a differential diagnosis or forme fruste of OFD syndrome suggests that an autosomal dominant pattern of inheritance should also be considered during genetic counseling.
Subject(s)
Orofaciodigital Syndromes , Polydactyly , Adolescent , Fingers/abnormalities , Fingers/pathology , Heart Septal Defects , Humans , Orofaciodigital Syndromes/diagnosis , Orofaciodigital Syndromes/genetics , Polydactyly/genetics , Toes/abnormalitiesABSTRACT
Oral-facial-digital syndromes (OFDSs) as a subgroup of ciliopathies are rare genetic disorders characterized by the association of abnormalities of the face, oral cavity, and extremities. OFDS XVII is a recently described subtype of OFDS that presents with developmental delay, facial dysmorphism, high palate, tongue nodules, brain malformations, cardiac anomaly, polydactyly, renal malformation, and various other findings. OFDS XVII is caused by biallelic variants in INTU gene and is inherited autosomal recessively. Intu is part of the CPLANE protein module that has an essential role in the ciliary transport system and function. INTU pathogenic variants have been reported in two patients with OFDS XVII, in two patients with short-rib thoracic dysplasia-20 with polydactyly (SRTD20), and one with nephronophthisis so far. We report the third family in the literature with OFDS XVII, with urogenital malformations as an additional finding.
Subject(s)
Orofaciodigital Syndromes , Polycystic Kidney Diseases , Polydactyly , Face/abnormalities , Humans , Orofaciodigital Syndromes/complications , Orofaciodigital Syndromes/diagnosis , Orofaciodigital Syndromes/genetics , Polydactyly/complications , ProteinsABSTRACT
Oral-facial-digital syndromes (OFDS) are a heterogeneous and rare group of Mendelian disorders characterized by developmental abnormalities of the oral cavity, face, and digits caused by dysfunction of the primary cilium, a mechanosensory organelle that exists atop most cell types that facilitates organ patterning and growth. OFDS is inherited both in an X-linked dominant, X-linked recessive, and autosomal recessive manner. Importantly, though many of the causal genes for OFDS have been identified, up to 40% of OFD syndromes are of unknown genetic basis. Here we describe three children with classical presentations of OFDS including lingual hamartomas, polydactyly, and characteristic facial features found by exome sequencing to harbor variants in causal genes not previously associated with OFDS. We describe a female with hypothalamic hamartoma, urogenital sinus, polysyndactyly, and multiple lingual hamartomas consistent with OFDVI with biallelic pathogenic variants in CEP164, a gene associated with ciliopathy-spectrum disease, but never before with OFDS. We additionally describe two unrelated probands with postaxial polydactyly, multiple lingual hamartomas, and dysmorphic features both found to be homozygous for an identical TOPORS missense variant, c.29 C>A; (p.Pro10Gln). Heterozygous TOPORS pathogenic gene variants are associated with autosomal dominant retinitis pigmentosa, but never before with syndromic ciliopathy. Of note, both probands are of Dominican ancestry, suggesting a possible founder allele.
Subject(s)
Alleles , Genetic Association Studies , Genetic Predisposition to Disease , Genetic Variation , Orofaciodigital Syndromes/diagnosis , Orofaciodigital Syndromes/genetics , Female , Genetic Testing , Genotype , Humans , Infant , Infant, Newborn , Magnetic Resonance Imaging , Male , Mutation , Neoplasm Proteins/genetics , Nuclear Proteins/genetics , Phenotype , Ubiquitin-Protein Ligases/genetics , Exome SequencingSubject(s)
Adaptor Proteins, Signal Transducing/genetics , Ciliopathies/diagnosis , Cleft Palate/diagnosis , Orofaciodigital Syndromes/diagnosis , Child , Child, Preschool , Ciliopathies/diagnostic imaging , Ciliopathies/genetics , Ciliopathies/pathology , Cleft Palate/diagnostic imaging , Cleft Palate/genetics , Cleft Palate/pathology , Female , Fetus/diagnostic imaging , Fetus/pathology , Humans , Hydrocephalus/diagnosis , Hydrocephalus/diagnostic imaging , Hydrocephalus/genetics , Male , Orofaciodigital Syndromes/diagnostic imaging , Orofaciodigital Syndromes/genetics , Orofaciodigital Syndromes/pathology , Prenatal Diagnosis/methodsABSTRACT
Orofaciodigital syndrome (OFDS) is a collective term for a rare inherited disorder that displays a wide phenotypic and genetic heterogeneity. The findings of diagnostic are the combination of the characteristic oral, facial and digital anomalies. In this heterogeneous group, the diagnosis of OFDI focuses on the association of the oro-dental, digital and cerebral malformations, polycystic kidney disease and several other manifestations. In this article, we report and discuss the case of a girl with OFDI syndrome, who presented as a peculiar phenotype on clinical examination. The present case was diagnosed at 24 months old and re-examined at 16 years old. The imagistic and cephalometric analyses were performed to investigate the alterations in the facial and skeletal bones and also neurological, renal and dental development. The differential diagnosis of this entity is discussed.
Subject(s)
Orofaciodigital Syndromes/diagnosis , Child, Preschool , Female , Humans , Orofaciodigital Syndromes/pathologySubject(s)
Adaptor Proteins, Signal Transducing/genetics , Cytoskeletal Proteins/genetics , Genetic Association Studies , Genetic Predisposition to Disease , Mutation , Orofaciodigital Syndromes/diagnosis , Orofaciodigital Syndromes/genetics , Phenotype , Alleles , Amino Acid Substitution , Biomarkers , Child, Preschool , Genotype , Humans , Male , RadiographyABSTRACT
Orofaciodigital syndrome 1 (OFD-1) is a rare, X-linked, dominantly inherited disorder caused by an OFD1 mutation that can cause polycystic kidneys. A 37-year-old woman on hemodialysis therapy was admitted to our hospital for trans-catheter arterial embolization therapy for enlarged polycystic kidneys. Lobulated tongue and brachydactyly were noticed, prompting an OFD1 sequencing analysis. Sequencing revealed a causal four-base-pair deletion in exon 13, both in the patient and in her mother, whose renal function had been retained. The peripheral leukocyte X chromosome inactivation pattern was skewed in the patient but not in her mother, suggesting some role in their phenotypic difference.
Subject(s)
DNA/genetics , Orofaciodigital Syndromes/genetics , Proteins/genetics , X Chromosome Inactivation/genetics , Adult , DNA Mutational Analysis , Exons , Female , Humans , Magnetic Resonance Imaging , Mothers , Mutation , Orofaciodigital Syndromes/diagnosis , Pedigree , Proteins/metabolism , Radiography, Panoramic , Sequence DeletionSubject(s)
Orofaciodigital Syndromes/diagnosis , Prenatal Diagnosis/methods , Abnormalities, Multiple/diagnosis , Abnormalities, Multiple/genetics , Abnormalities, Multiple/pathology , Female , Gestational Age , Humans , Magnetic Resonance Imaging , Male , Membrane Proteins/genetics , Mutation , Orofaciodigital Syndromes/genetics , Orofaciodigital Syndromes/pathology , Pregnancy , Pregnancy Trimester, Second , Siblings , Ultrasonography, PrenatalABSTRACT
Orofaciodigital syndrome type I and X-linked recessive Joubert syndrome are known ciliopathic disorders that are caused by pathogenic variants in OFD1 gene. Endocrine system involvement with these conditions is not well described. We present the first report of a newborn male with a novel hemizygous variant in OFD1 gene c.515T>C, (p.Leu172Pro) resulting in X-linked Joubert syndrome and orofaciodigital features with complete pituitary gland aplasia and subsequent severe hypoplasia of peripheral endocrine glands. This clinical report expands the phenotypic spectrum of endocrine system involvement in OFD1-related disorders and suggests that OFD1 gene may be related to pituitary gland development.
Subject(s)
Abnormalities, Multiple/diagnosis , Abnormalities, Multiple/genetics , Cerebellum/abnormalities , Eye Abnormalities/diagnosis , Eye Abnormalities/genetics , Genes, X-Linked , Kidney Diseases, Cystic/diagnosis , Kidney Diseases, Cystic/genetics , Mutation , Phenotype , Proteins/genetics , Retina/abnormalities , Alleles , Genotype , Humans , Infant, Newborn , Magnetic Resonance Imaging , Male , Orofaciodigital Syndromes/diagnosis , Orofaciodigital Syndromes/genetics , Pedigree , Pituitary Gland/abnormalities , Radiography , Exome SequencingSubject(s)
Acne Vulgaris/genetics , Agenesis of Corpus Callosum/genetics , Orofaciodigital Syndromes/genetics , Proteins/genetics , Acne Vulgaris/etiology , Agenesis of Corpus Callosum/diagnostic imaging , Agenesis of Corpus Callosum/etiology , Female , Frameshift Mutation , Humans , Infant , Lateral Ventricles/abnormalities , Lateral Ventricles/diagnostic imaging , Orofaciodigital Syndromes/complications , Orofaciodigital Syndromes/diagnosisABSTRACT
Mutations in CPLANE1 (previously known as C5orf42) cause Oral-Facial-Digital Syndrome type VI (OFD6) as well as milder Joubert syndrome (JS) phenotypes. Seven new cases from five unrelated families diagnosed with pure OFD6 were systematically examined. Based on the clinical manifestations of these patients and those described in the literature, we revised the diagnostic features of OFD6 and include the seven most common characteristics: 1) molar tooth sign, 2) tongue hamartoma and/or lobulated tongue, 3) additional frenula, 4) mesoaxial polydactyly of hands, 5) preaxial polydactyly of feet, 6) syndactyly and/or bifid toe, and 7) hypothalamic hamartoma. By whole or targeted exome sequencing, we identified seven novel germline recessive mutations in CPLANE1, including missense, nonsense, frameshift and canonical splice site variants, all causing OFD6 in these patients. Since CPLANE1 is also mutated in JS patients, we examined whether a genotype-phenotype correlation could be established. We gathered and compared 46 biallelic CPLANE1 mutations reported in 32 JS and 26 OFD6 patients. Since no clear correlation between paired genotypes and clinical outcomes could be determined, we concluded that patient's genetic background and gene modifiers may modify the penetrance and expressivity of CPLANE1 causal alleles. To conclude, our study provides a comprehensive view of the phenotypic range, the genetic basis and genotype-phenotype association in OFD6 and JS. The updated phenotype scoring system together with the identification of new CPLANE1 mutations will help clinicians and geneticists reach a more accurate diagnosis for JS-related disorders.
Subject(s)
Abnormalities, Multiple/genetics , Cerebellum/abnormalities , Eye Abnormalities/genetics , Germ-Line Mutation , Kidney Diseases, Cystic/genetics , Membrane Proteins/genetics , Orofaciodigital Syndromes/genetics , Retina/abnormalities , Abnormalities, Multiple/diagnosis , Adolescent , Adult , Child , Child, Preschool , Eye Abnormalities/diagnosis , Female , Humans , Infant , Infant, Newborn , Kidney Diseases, Cystic/diagnosis , Male , Middle Aged , Orofaciodigital Syndromes/diagnosis , PenetranceABSTRACT
Orofaciodigital syndrome (OFD) is a group of hereditary disorders identified by malformations of the mouth (oris), face (facies), hands and feet (digitus=finger and toe). Although there are several different types reported in the literature, there is a great overlap in their clinical presentation. The full spectrum of all disorders due to OFD is not yet fully understood, since each patient shows variations in the expression of the syndrome. In the oral cavity, teeth are often affected by various alterations, such as dental caries, abnormal teeth, enamel hypoplasia, supernumerary teeth and dental agenesis. Treatment of a syndromic patient with a complex picture showing conditions such as palatine fissures and a severe hypodontia involves a multidisciplinary approach and a careful periodical follow-up.
Subject(s)
Orofaciodigital Syndromes/diagnosis , Orofaciodigital Syndromes/therapy , Dental Caries , Dental Enamel Hypoplasia , Follow-Up Studies , Humans , Tooth, SupernumeraryABSTRACT
The oral-facial-digital syndrome belongs to a group of hereditary diseases, manifested by multiple birth defects (usually, the face and fingers). At the current stage, there are 14 genetic variations of the oral-facial-digital syndrome. The presence of various abnormalities of the oral cavity, face and fingers is common for all of them, but each syndrome has a specific phenotype or type of inheritance. The etiology of this syndrome is unknown. It is inherited in an X-linked dominant pattern. Aim of the study: to describe and analyze the clinical case of oral-facial-digital syndrome. Data of the patient (Kira M., 11 months old): clinical-anamnestic examination, chest radiography, ultrasound investigation, molecular-genetic testing OFD1. Results Numerous miliae are detected on the face and ears of the child. Facial dysmorphy (large wide eyes, epicantus, wide nose bridge, telecantus, small mouth, small beak shaped nose, hypoplasia of the wings of the nose, small chin). The large fontanel is closed. Focal alopecia and dry hair are noted. Syndactyly of 2nd-3rd toes, asymmetrical shortening of the index finger of the right hand. Oral cavity examination reveals cleft palate, ankyloglossy and tongue lobulation. Transcranial ultrasonography: M echodex = 50.0 mm. M echosin = 52.0 mm. VIII = 6.9 mm (N up to 3.0 mm). V latdex = 24.4 mm, V latsin = 25.0 mm (N up to 16.0 mm). Neurologist's consultation: "Congenital brain malformation: agenesis of corpus callosum, congenital cerebral cysts." Ultrasound examination of the abdominal organs detected liver enlargement (anteroposterior size of the right lobe: 78 mm (N up to 65 mm), left lobe: 0.38 mm (+1.5 cm) Conclusion Oral-facial-digital syndrome type I is an inherited pathology, which in most cases is diagnosed immediately after birth on the basis of oral, facial and digital anomalies. Molecular genetic study makes it possible to confirm this disease and provide counseling to family members. Elimination of some developmental defects (hard palate plastic, correction of frenulum hyperthrophy), as well as a properly selected complex of therapeutic and rehabilitation measures greatly improves the quality of life of the patient and contributes to a favorable forecast.
Subject(s)
Orofaciodigital Syndromes/diagnosis , Pneumonia, Bacterial/complications , Anti-Bacterial Agents/therapeutic use , Anti-Inflammatory Agents/administration & dosage , Anti-Inflammatory Agents/therapeutic use , Female , Humans , Infant , Mutation , Orofaciodigital Syndromes/complications , Orofaciodigital Syndromes/genetics , Orofaciodigital Syndromes/therapy , Pneumonia, Bacterial/drug therapy , Proteins/genetics , Quality of Life , Treatment OutcomeABSTRACT
Numerical anomalies, either addition or deletion, are quite a common findings in human dentition. However, it is extremely rare to find both hypodontia and hyperdontia simultaneously in the same individual. This condition is referred as concomitant hypohyperdontia (CHH). Aetiology of this condition is still obscure. The prevalence of CHH has been reported to be between 0.002% and 3.1%. This case report highlights a rare occurrence of bimaxillary CHH represented by the absence of both mandibular central incisors and presence of two supernumerary teeth in the maxillary anterior segment. The rarity of such condition of mixed hypodontia as well as hyperdontia in single human dentition prompted the author to report the case.