https://doi.org/10.5812/mejrh.97231

Oromandibular Limb Hypogenesis Syndrome Type I B as a Rare Clinical Variant: A Case Report and Review of the Literature

authors:

avatar Azam Hosseini 1 , avatar Shabnam Sohanian ORCID 2 , *

Oral Medicine Department, Dental School, Semnan University of Medical Sciences, Semnan, Iran
Oral and Maxillofacial Pathology Department, Dental School, Semnan University of Medical Sciences, Semnan, Iran
Middle East Journal of Rehabilitation and Health Studies: Vol.7, issue 1; e97231
published online: December 18, 2019
article type: Case Report
received: August 16, 2019
revised: September 26, 2019
accepted: November 14, 2019

How To Cite Hosseini A, Sohanian S. Oromandibular Limb Hypogenesis Syndrome Type I B as a Rare Clinical Variant: A Case Report and Review of the Literature. Middle East J Rehabil Health Stud. 2020;7(1):e97231. https://doi.org/10.5812/mejrh.97231.

Abstract

Introduction:

Hypoglossia-hypodactyly is an uncommon genetic abnormality affecting the tongue and limbs. First, it was classified under a multipart group of disorders called oromandibular limb hypogenesis syndromes. The most extensively accepted etiology is intrauterine trauma. Hypoglossia, micrognathia of the mandible, and limb anomalies are the characteristic features of the syndrome.

Case Presentation:

A 19-year-old female patient was admitted to the Oral Medicine Department of the Dental School, Semnan University of Medical Sciences, for a dental checkup. After obtaining informed consent, the necessary dental prophylaxis was performed. This case was unique because the patient had only aglossia and deformity in her right hand and fingers.

Conclusions:

Since the disease is rare and presents as the first case in Iran, dentists must have knowledge about its clinical features and proper patient management. They also should explain the significance of systematic dental checkups, perfect oral hygiene, and the use of regular fluoride to patients. Therefore, the awareness of dentists is essential about diagnosis and appropriate referral to specialists.

1. Introduction

Oromandibular limb hypogenesis syndrome (OLHS) is a very rare disease characterized by a variety of disorders affecting the tongue and limbs (1). Although its etiology is still unknown, both genetic and environmental factors have been suggested as etiological factors. However, the most commonly accepted etiology is exposure to environmental factors during pregnancy such as maternal hyperthermia, radiation, medicines, and nutritional deficiencies (2). Some drugs such as diazepam and chlorpromazine are involved in the causation of OLHS, but their effects have not yet been proven (3-5). Individuals who suffer from this syndrome frequently display overlapping clinical manifestations such as aglossia, hypoglossia, adactyly, and hypodactyly (2). Three features that are necessary for the diagnosis of the syndrome include (1) variable size of the tongue (microglossia), (2) micrognathia of the jaw in the midline segment, and (3) varying severity of limb anomalies (3).

Aglossia is a particularly rare genetic disorder accompanying with inherited malformations such as microcephaly, adactylia, mental retardation, hypodactylia, deafness, palatal cleft, hypodontia, and anodontia (3). Rosenthal (6) first reported the occurrence of aglossia and adactylia.

Limb anomalies have a particularly variable range from syndactyly, referring to the partial separation of fingers, to amelia, referring to the missing of the limb (3). Generally, they tend to be distal to humerus and femur (1). Different variations may be seen in one or more limbs in the same patient or in different individuals (1, 3). There are some visceral anomalies associated with this syndrome including the imperforate anus, ileal atresias, absence of a kidney, and fused labia majora (3).

The best classification to describe hypoglossia and limb deformity in OLHS was declared by Hall (7). Nevertheless, Hall’s classification cannot categorize aglossia and other associated abnormalities.

Here we present a patient with oromandibular malformations associated with a defect in her right hand and aglossia (aglossia-adactylia).

2. Case Presentation

A 19-year-old female patient was admitted to the Oral Medicine Department of the Dental School, Semnan University of Medical Sciences, for a dental checkup. The patient had microstomia, misaligned teeth, and problems in speech but had no difficulty in swallowing and breathing. The patient was the third child of her parents who had four children. There was no history of similar results in the family and the parents had no history of consanguineous marriage.

On the general examination, she had no unusual finding except for deformity in her right upper limb with five nubbins attached to its distal part (Figure 1). The intraoral examination revealed microstomia, incompetent lips, constricted maxillary and mandibular arches, crowding in upper and lower anterior teeth, aglossia, and hypodontia. After a thorough evaluation of the patient, we arrived at a final diagnosis of oromandibular-limb hypogenesis syndrome type IB.

Deformity in the right upper limb with five nubbins attached to its distal part
Deformity in the right upper limb with five nubbins attached to its distal part
Figure 1.

Deformity in the right upper limb with five nubbins attached to its distal part

Oral prophylaxis was performed after obtaining informed consent. The significance of systematic dental checkup, perfect oral hygiene, and the regular use of fluoride was explained to the patient.

3. Discussion

Oromandibular-limb hypogenesis syndrome is characterized by a variety of complaints affecting the tongue and limbs. These patients frequently have overlapping clinical features. Therefore, this complex syndrome has been classified to clarify the diagnosis (2). Hall’s classification (7) is the best one to describe limb anomalies as presented in our patient. Consequently, our case was diagnosed with OLHS type 1-B2: Aglossia with adactylia.

Hall classified OLHS into five groups only with the essential principles of hypoglossia and limb defect. However, some authors reported cases that showed aglossia related to limbs and other congenital malformations (1). Preis et al. (8) remarked aglossia accompanying hypodactylia, anodontia, ventricular septal defect, epidermoid of the right eye, and paresthesia of the sixth and seventh cranial nerves. Recently, Kantaputra and Tanpaiboon (9) revealed the relationship between aglossia and microstomia, partial anodontia, mental retardation, microcephaly, and hypothyroidism. Higashi and Edo (10) reported the association of aglossia with conduction deafness. Here we present a case that showed an association between aglossia and hypodactylia. This case is the first reported OLHS case in Iranian literature. Therefore, it is necessary to supplementarily categorize Hall’s classification established on aglossia and hypoglossia. Kalaskar et al. (2) recommended modifications for Hall’s classification type IB (Table 1).

Table 1.

Modification of Type I B Hall’s Classification

Hall’s ClassificationModified SubtypesClinical FeaturesReferences
Type I B (Aglossia)Type I-B1Isolated aglossiaSalles et al. (11), Gupta (12)
Type I-B2Aglossia with adactyliaNevin et al. (1), Purohit et al. (13)
Type I-B3Aglossia with hypodactylia (mental retardation, cardiac defect, anodontia, hypothyroidism)Preis et al. (8), Kantaputra and Tanpaiboon (9)
Type I-B4Aglossia with rudimentary ear (deafness)Higashi and Edo (10), Kalaskar et al. (2)

Both genetic and environmental factors have been mentioned as the OLHS etiology (4). A few reported cases had intrafamilial histories, but most reported cases were sporadic (3, 4). There has been no genetic mutation or chromosomal abnormalities for this syndrome to date (3, 4). However, the suggested etiologies include maternal hyperthermia, heredity, and positive drug history during pregnancy (14). Several authors have recommended that the use of numerous drugs such as meclizine, marijuana, and benzamide hydrochloride during pregnancy is the reason for this syndrome, but none has been proven (15).

During embryonic development, the anterior tongue is formed from the first branchial arch and the posterior part is created from the second and the third branchial arches. Therefore, hypoglossia is attributed to the failed growth of these three branchial arches (15-17).

Sucking, swallowing, taste, speech, perception, mastication, development of jaws and occlusion are the important functions of the tongue. Though the tongue is deficient or absent, activities such as swallowing and speech improve with time in the majority of the cases. This is conceivable by adaptive mechanisms of the orofacial assembly, which helps in swallowing, taste sensation, and feeding and improves speech (12, 14).

For maintenance of such patients, appropriate preventive procedures are essential including oral prophylaxis, fluoride therapy, and pit and fissure sealants. However, the complete rehabilitation of individuals with aglossia is complicated and necessitates a multidisciplinary approach. Surgical and orthodontic treatment would be required to correct jaw anomalies and malocclusion (15). Consequently, timely diagnosis, constant maintenance, and a multidisciplinary approach are mentioned for the supervision of such patients.

3.1. Conclusions

Since this disease is rare and presents as the first case in Iran, dentists must have knowledge about its clinical features and proper patient management. They also should explain the significance of systematic dental checkup, perfect oral hygiene, and the use of regular fluoride to the patient. Therefore, the awareness of dentists about diagnosis and appropriate referral to specialists is essential.

References