Restoration of a malformed primary incisor using digital technology in a pediatric patient with congenital Zika virus syndrome: A case report.

Zika virus congenital syndrome (ZVCS) is a congenital viral infection resulting from the transmission of the Zika virus (ZV) to the fetus during pregnancy. This report describes a clinical case involving a 20-month-old female child with ZVCS, who presented with systemic changes related to the syndrome, such as microcephaly, arthrogryposis, ocular and auditory changes, and oral changes such as delayed dental eruption, ogival (high-arched) palate, short lip frenum, and altered morphology of a superior primary incisor. For esthetic and functional rehabilitation of the oral health of this child, an indirect composite resin restoration was performed using intraoral digital scanning technology. This case presents an accurate, rapid, and comfortable restorative treatment option that might result in excellent outcomes in children with ZVCS or similar syndromes with neurological impairment.

Infantile hypothyroidism and its relationship with delayed tooth eruption: A case report.

Hypothyroidism is characterized as a systemic endocrine disorder that is caused by a dysfunction of the thyroid gland. This produces the thyroid hormones T3 and T4 that are responsible for carrying out the normal functions of the physical body, that is, changes in the secretion of these hormones may be related to some maladjustments in the stomatognathic system. The most common manifestations of congenital hypothyroidism, also known as cretinism, are thick lips, macroglossia, malocclusion and delayed eruption of both dentitions. This study aims to report a case of a child with hypothyroidism and a delay in the chronology of tooth eruption. Patient, female, 9 years and 8 months old, whose main complaint was a delay in the chronology of tooth eruption. On clinical examination, a marked delay in the chronology of tooth eruption was observed. Therefore, it was necessary to refer the patient to a geneticist, who ruled out any syndromic alteration. Then, the patient was referred to the endocrinologist, whose opinion was hypothyroidism. Key words:Hypothyroidism, tooth eruption, endocrine disorder, child health.

Generalized odontodysplasia in a 5-year-old patient with Hallermann-Streiff syndrome: clinical aspects, cone beam computed tomography findings, and conservative clinical approach.

This article aims to report the main clinical aspects, cone beam computed tomography (CBCT) findings, and conservative oral rehabilitation in a child born from a consanguineous marriage who presented with Hallermann-Streiff syndrome (HSS) and generalized odontodysplasia. A 5-year-old girl presented with a diagnosis of HSS for oral evaluation. Radiographically, all teeth showed wide pulp chambers and roots with thin dentinal walls and open apices, resembling ghost teeth and indicating a diagnosis of odontodysplasia. Oral rehabilitation consisted of partial dentures that were regularly adjusted to conform the device with the pattern of growth and development of the child. CBCT scan provided great insight into HSS, allowing a detailed view of the morphologic aspects and associated trabecular bone pattern. Treatment of these 2 rare conditions in young children must consider the stage of growth and development. Although extremely rare in HSS, odontodysplasia should be investigated and conservatively managed in young children.

Cephalometric characteristics and dentofacial abnormalities of pycnodysostosis: report of four cases from Brazil.

Pycnodysostosis (PKND) is a human autosomal recessive genetic disorder characterized mainly by osteosclerosis of the skeleton, severe bone fragility, and short stature. This syndrome usually presents very typical craniofacial deformities, such as beaked nose, micrognathia, hypoplastic midface, open mouth posture, grooved palate, anterior cross-bite, dental crowding, and over-retained deciduous teeth. Early diagnosis and intervention are of the utmost importance. Four cases from the northeast of Brazil are reported including 2 siblings. Features included maxillary retrusion, reduced facial height, open bite, and bone fracture history. Very poor oral hygiene, severe dental caries, and periodontal disease were also present.