Exam 2 - Clinical Scenarios and Other Notes Flashcards
Neurocranium vs Viscerocranium
Neuro: cartilaginous neurocranium cradles skull in the first 10 weeks, then forms the membranous neurocranium
Viscerocranium: cartilaginous (first branchial arch cartilage - Meckels, second arch - Reicherts, third, fourth, and sixth) and membranous components too (maxillary and mandibular prominence of first branchial arch)
Cranioschisis (acrania)
Failure of the occipital and parietal bones to completely form or close
Associated with arrested brain development and rudimentary forebrain (anencephaly)
Microcephaly vs Macrocephaly
Micro: small cranium due to fusion of cranial structures
Macro: enlarged secondary to hydrocephalus
Craniosynostosis
One or more of the fibrous sutures in an infant skull prematurely fuses by turning into bone, thereby changing growth pattern
Development from Morula to Embryo
Morula: dense ball of cells
Blastocyst: divided into inner cell mass and hypoblasts
Bilaminar embryo: epiblasts and hypoblasts
Gastrulation occurs at this level to form the embryo
Places where mesenchymal cells will not invade:
Prochordal plate (mouth) and cloacal membrane
At four weeks, the embryo will have:
Stomodeum (mouth) surrounded by five facial swellings of the first branchial arch
- includes the frontal, maxillary, and mandibular prominences
Buccopharyngeal Membrane
Divides the anterior 2/3 and posterior 1/3 of the tongue (supplied by GVE)
Development of the face occurs during:
Weeks 5-10
Maxillary Prominence forms:
Lateral parts of the upper lip, jaw, and secondary palate or palatine shelves
Mandibular Prominence forms:
Lower jaw and lips
If the mandibular prominence fails to fuse:
Cleft chin
Development of the Nasal Cavity
- Nasal pits deepen to form primitive nasal cavity
- Medial nasal prominences Duse as intermaxillary process
- Intermaxillary process forms nasal septum and primary palate
Formation of the Palate occurs:
Weeks 5-12
Mid-posterior landmark between the palates:
Incisive Foramen (Foramen of Cecum)
Formation of the Secondary Palate
Formed by shelf-like projections, lateral palatine processes or palatine shelves
appears at week 6
Anterior Cleft Deformity
Caused by a failure of medial nasal and maxillary swellings to fuse
Can be unilateral or bilateral - if bilateral, will see the intermaxillary prominence in between the two clefts
Posterior Cleft Deformity
Caused by the palatine shelves not fusing during development
Usually unilateral
Cleft Lip vs Cleft Palate
Cleft lip is more prominent and occurs more frequently in males
- maternal age may play a role in occurrence
Cleft palate is more frequent in females
no genetic relationship between cleft lip and isolated cleft palate
Oblique Facial Cleft
Caused by failure of maxillary swelling to merge with its corresponding lateral nasal swelling
Nasolacrimal duct is exposed - may have phonation issues
Median Cleft Lip and Bifid Nose
Caused by failure of medial nasal prominences to fuse
very rare, may be autosomal recessive
Macrostomia vs Microstomia
Dysfusion of the maxillary and mandibular swellings
Macro: will have a very wide mouth
Agathnia
Dysgenesis of the mandibular swelling
- first branchial arch
- position of the auricle
- congenitally deaf
Holoprosencephalic
Includes cyclopia, cebocephaly, defect of the midface
Weeks 5, 6, 7, and 10
may be associated with fetal alcohol syndrome