Anatomy of Hard and Soft Palate: Bones, Muscle, Artery, and Nerves
The hard and soft palate is composed of bone and soft tissue. This article details structures, neuromuscular supply and abnormal anatomy.
The hard and soft palate is composed of bone and soft tissue. This article details structures, neuromuscular supply and abnormal anatomy.
This assesses your clinical expertise, decision-making, and management skills through an oral "viva" structure, using real-world scenarios representative of clinical practice and exams.
This assesses your clinical expertise, decision-making, and management skills through an oral "viva" structure, using real-world scenarios representative of both practice and exams.
This assesses your clinical expertise, decision-making, and management skills through an oral "viva" structure, using real-world scenarios representative of both practice and exams
This assesses your clinical expertise, decision-making, and management skills through an oral "viva" structure, using real-world scenarios representative of both practice and exams
This assesses your clinical expertise, decision-making, and management skills through an oral "viva" structure, using real-world scenarios representative of clinical practice and exams
This journal club analyses and reviews the original publication by Mustarde for the correction of prominent ears.
Polydactyly is the radial, ulnar, or central duplication of digits. This article details the classification, treatment, and aetiology of this congenital condition.
Upper Limb development occurs during weeks 4-8 of gestation. This article details the mechanisms of development and critical milestones.
Camptodactyly is the progressive flexion deformity of the PIPJ. This article details the aetiology, features, classification, and management of this congenital hand condition.
Syndactyly is the fusion of soft tissue and bone of the finger. This article details the aetiology, diagnosis, and treatment of syndactyly.
Thumb hypoplasia is congenital undergrowth of the thumb. This article details its diagnosis, classification, and treatment.
Craniosynostosis is the premature fusion of one or more cranial sutures. It most commonly involves the sagittal suture. It can be isolated or part of a syndrome.
Microtia is a congenital hypoplastic malformation of the ear. This article details the assessment, classification, and surgical management of microtia.
Pharyngeal arches (branchial arches) provide nerve, artery, bone and muscle to the craniofacial development. This article explores arches, pouches and grooves.
Infantile haemangiomas are benign proliferative tumours. This article details their aetiology, clinical features, investigations and management.
This assesses your clinical expertise, decision-making, and management skills through an oral "viva" structure, using real-world scenarios representative of clinical practice and exam
This assesses your clinical expertise, decision-making, and management skills through an oral "viva" structure, using real-world scenarios representative of clinical practice and exam
Cleft hand is a central longitudinal congenital deficiency. This article details the aetiology, features, classification and treatment.
Congenital Melanocytic Naevi are pigmented lesions present at birth. This article details clinical features, management and risk of malignancy.
Treacher Collins Syndrome is a genetic craniofacial syndrome characterised by hypoplasia, external ear and eyelid malformations and visual disturbance.
Pierre Robin Sequence is glossoptosis, micrognathia and upper airway respiratory obstruction. This article details pathophysiology, causes and treatment.
Hemifacial microsomia is the commonest craniofacial abnormality. This article details the genetics, clinical features, classifications and management.
Craniofacial Distraction Osteogenesis is a key principle in paediatric craniofacial surgery. These articles explores techniques, types, biology & indications
5 Key Points – Velopharnygeal Insufficiency Velopharyngeal Insufficiency and its aetiology, clinic picture, diagnosis and management can be summarised in 5
Van der Woude syndrome is a rare autosomal dominant disorder characterised by lower lip pits and cleft lip with or without cleft palate. Clinical presentation is variable because of the autosomal dominant inheritance with incomplete penetrance. Management is a multidisciplinary approach.
Surgical techqniues for Otoplasty are well-described. They are best understood by classifying them into manouvres aimed at correcting prominent ears.
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