Craniodentofacial Manifestations In Hallermann-Streiff Syndrome

Tuna, Elif-Bahar; Sülün, Tonguç; Rosti, Ozgur; Abdallah, Fouad El; Kayserili, Hülya; Aktören, Oya

doi:10.1179/crn.2009.006

Cited by 14 publications

(6 citation statements)

References 9 publications

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“…[42] Dental abnormalities, such as malocclusion, severe caries, enamel hypoplasia, supernumerary and neonatal teeth, hypodontia, and premature eruption of primary teeth, are present in 80% of patients with this syndrome. [42]…”

Section: Resultsmentioning

confidence: 99%

“…Chromosomal and genetic abnormalities or congenital anomalies [40][41][42] Not applicable Chronic (or congenital Articular disc fracture (bilateral case). Bilateral cases cause an anterior open bite with clockwise rotation of the mandible.…”

Section: Othersmentioning

confidence: 99%

“…[41] Hallermann-Streiff syndrome is characterized by dyscephaly, short stature, bilateral microphthalmia, cataracts, hypotrichosis, and skin atrophy. [42] Dental abnormalities, such as malocclusion, severe caries, enamel hypoplasia, supernumerary and neonatal teeth, hypodontia, and premature eruption of primary teeth, are present in 80% of patients with this syndrome. [42]…”

Section: Dislocation (Bilateral Case) Bilateral Dislocation Causesmentioning

confidence: 99%

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Can malocclusion provide clinicians with information for differential diagnosis of temporomandibular joint diseases?: A review

et al. 2022

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The aim of this literature review was to summarize the clinical characteristics and symptoms of temporomandibular joint diseases, and to discuss the associations between temporomandibular joint diseases and categorization of malocclusion. Electronic literature searches were performed using the PubMed database. The authors established a differential diagnostic method for temporomandibular joint diseases related to malocclusion. A literature search using PubMed yielded 213 texts, of which based on exclusion criteria, 28 were included in this study. Malocclusions were categorized into 5 types. The authors suggested a diagnostic tree of temporomandibular joint diseases based on the types of malocclusion and 4 variables in clinical characteristics and symptoms. Clinicians treating malocclusions must attempt to clarify the cause of the occlusal condition. If caused by temporomandibular joint disease, it is important to make a proper differential diagnosis at first, and not to overlook the causative disease. Further clinical knowledge of associations between temporomandibular joint diseases and malocclusions should be accumulated, and the diagnostic tree should be improved based on new information.

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Section: Resultsmentioning

confidence: 99%

Section: Othersmentioning

confidence: 99%

Section: Dislocation (Bilateral Case) Bilateral Dislocation Causesmentioning

confidence: 99%

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Can malocclusion provide clinicians with information for differential diagnosis of temporomandibular joint diseases?: A review

et al. 2022

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“…Al-Awadi/Raas-Rothschild syndrome and Goldenhar syndrome (Camera, Ferraiolo, Leo, Spaziale, & Pozzolo, 1993;da Silva Dalben, Costa, & Gomide, 2006;Tuna et al, 2011), while narrow mouth is present in other syndromes like Hallermann-Streiff syndrome and mandibuloacral dysplasia (Amr, Mostafa, & El-kamah, 2012;Tuna et al, 2009).…”

Section: Discussionmentioning

confidence: 99%

Philtrum length and intercommissural distance measurements at mixed dentition period

Mostafa

Hassib

Sayed

et al. 2018

American J of Med Genetics Pt A

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Anthropometric measurements of the lip and mouth are of great importance in clinical dysmorphology as well as reconstructive plastic surgery. In this study, the philtrum length (PhL) and intercommissural distance (ICmD) nomograms for Egyptian children in the mixed dentition period were established. A group of 1,338 Egyptian students in primary schools (735 boys and 603 girls) were included in the study. The students were at mixed dentition period and their ages ranged from 7 to 12 years. Anthropometric norms of PhL and ICmD were developed with significant sex difference in certain groups. A ratio between PhL and ICmD was developed. These data will help facilitate both objective and subjective evaluation of the lip and mouth for proper diagnosis of orofacial anomalies and variations as well as for ideal treatment plans.

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“…Hallermann-Streiff syndrome (OMIM 234100): In a 10-year-old girl the mandible had reduced length and was posteriorly placed, resulting in a skeletal and dental class II. In the vertical plane, the patient presented a vertical growth pattern with an opening of the gonial angle, a large anterior open bite, and an excessive increase in the lower anterior facial heigh [99]t.…”

Section: Q112 Deletion Syndrome (Omim 611867)mentioning

confidence: 99%

Cephalometric Evaluation of Children with Short Stature of Genetic Etiology. A Review

Paltoglou,

Ziakas,

Chrousos

et al. 2024

Preprint

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Introduction: A plethora of biological molecules regulate chondrogenesis in the epiphyseal growth plate. Disruptions of quantity and function of these molecules can manifest clinically as stature abnormalities of various etiologies. Traditionally, the growth hormone/insulin-like growth factor 1 (IGF1) axis represents the etiological center of final stature attainment. Of note, little is known about the molecular events that dominate the growth of the craniofacial complex and its correlation with somatic stature. Aim: Given the paucity of the relevant data, this review discusses available information regarding potential applications of lateral cephalometric radiography as a potential clinical indicator of genetic short stature in children. Materials and Methods: A literature search was conducted in the PubMed electronic database using the key words: cephalometric analysis and short stature; cephalometric analysis and achondroplasia; cephalometric analysis and hypochondroplasia; cephalometric analysis and skeletal abnormalities; cephalometr* and SHOX; cephalometr* and CNP; cephalometr* and ACAN; cephalometr* and CNVs; cephalometr* and IHH; cephalometr* and FGFR3; cephalometr* and Noonan syndrome; cephalometr* and “Turner syndrome”; cephalometr* and achondroplasia. Results: In individuals with genetic syndromes causing short stature, linear growth of the craniofacial complex is confined, following the pattern of somatic short stature regardless of its etiology. The angular cephalometric measurements differ from the average height normal individuals and are suggestive of a posterior placement of the jaws and a vertical growth pattern of the face. Conclusion: The greater part of the existing literature regarding cephalometric measurements in short statured children with genetic syndromes provides qualitative data. Furthermore, cephalometric data for individuals affected with specific rare genetic conditions causing short stature, should be the focus of future studies. These quantitative data are required to potentially establish cut-off values to refer for genetic testing based on craniofacial phenotypes.

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Craniodentofacial Manifestations In Hallermann-Streiff Syndrome

Cited by 14 publications

References 9 publications

Can malocclusion provide clinicians with information for differential diagnosis of temporomandibular joint diseases?: A review

Can malocclusion provide clinicians with information for differential diagnosis of temporomandibular joint diseases?: A review

Philtrum length and intercommissural distance measurements at mixed dentition period

Cephalometric Evaluation of Children with Short Stature of Genetic Etiology. A Review

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