purpose: to describe the clinical findings, preoperative radiologic findings and results of surgery in a patient with congenital bilateral hypoplasia of medial rectus muscle case report: a 50-year-old man presented with large angle incomitant horizontal deviation with marked deficit of adduction of both eyes. mri finding defined very thin medial rectus muscle. intraoperatively medial rectus mus...

INTRODUCTION Tuberous breast deformity is one of the most challenging congenital breast anomalies. Severe forms present as hypoplasia of lower medial and lateral quadrants and breast base constriction. We present a modified technique based on redistribution of breast tissue for single-stage aesthetic correction of this deformity. MATERIAL METHODS AND SURGICAL TECHNIQUE The technique is based ...

Radiation therapy is used in the management of a number of childhood cancers and can have significant effects on skeletal growth. We present the case of a 35-year-old woman who developed a hypoplastic pelvis and buttocks following radiotherapy for rhabdomyosarcoma of the vagina at the age of 2. At the age of 25, the patient underwent bilateral buttock augmentation with a two-stage reconstructio...

The purpose of this study was to assess the longitudinal relationships between enamel hypoplasia and caries experience of primary second molars. The study sample was 491 subjects who received dental examinations at both age 5 and 9 by the calibrated examiners. Four primary second molars (n = 1,892) were scored for the presence of enamel hypoplasia for each participant. Caries presence and numbe...

Renal hypoplasia refers to a congenitally small kidney where there is essentially normal residual parenchyma but smaller calyces, lobules, and papillae. This anomaly can be divided into two broad groups: complete (global) renal hypoplasia and segmental renal hypoplasia. In this study, a 3 days-old simmental calf was diagnosed with renal hypoplasia and unreconstructed exstrophic bladder. It pres...

Goltz syndrome or focal dermal hypoplasia is a rare syndrome with mesoectodermal hypoplasia. This syndrome is an X-linked dominant disorder with involvement of the cutaneous, ocular, dental and skeletal systems. The most significant feature of this disease is connective tissue dysplasia. Here, we report a 30-year old woman who presented with congenital unilateral linear atrophic areas on her tr...

binder’s syndrome is an uncommon entity characterized by midfacial hypoplasia along with class iii incisal relationship. the individuals with this syndrome are easily recognizable and the syndrome is mostly associated with other malocclusions. the current article presents two cases of this rare syndrome and describes its general features. key words: binder’s, midfacial hypoplasia, maxillofacial...

150 Maxillary sinus hypoplasia (MSH) is the underdevelopment of maxillary sinus antrum and it is usually associated with other anomalies, such as uncinate process and infundibular passage. Hypoplasia is classified into three: Type I is mild hypoplasia, normal uncinate and infundibulum; Type II is significant hypoplasia with hypoplastic or absent uncinate and pathological infundibular passage; T...

AIMS Levels of enamel hypoplasia in past populations are frequently used to study health. However, few studies have looked at patterning in the occurrence of different types of hypoplasia. In this pilot study, skeletal remains from an Iron Age tomb at Pella in Jordan were analysed for the presence of linear and pit enamel hypoplasia, to investigate enamel hypoplasia aetiology by comparison of t...