HEAD
Head
Always Remove The Cap
Occipito-Frontal Circumference
Microcephaly & Macrocephaly
Microcephaly – OFC < 2SD
Macrocephaly – OFC > 2SD
Fontanelle
Junction of >2 flat bones
Anterior fontanelle
Junction of metopic, sagittal, and coronal sutures.
Diamond shaped - 1-4cm.
Posterior fontanelle
Junction of the sagittal and lambdoid sutures, <1 cm
Tense and bulging fontanelle
Raised intracranial pressure (ICP)
Sutures
To Check
Wide Suture - > 1cm
Congenital Hypothyroidism
Down Syndrome
Achondroplasia
Increased Intracranial Pressure
Moulding �Vs �Craniosynostosis
Craniosynostosis:�Premature fusion of sutures
One suture closes early & remaining continue growing, resulting in:
An Abnormally Shaped Skull
Lack Of Room For The Brain To Grow
Raised intra-cranial pressure.
Primary or Secondary
Simple (one suture Involved) Or Compound (multiple sutures involved)
Craniotabes
Soft area of skull bone, usually in the parietal region.
Seen in:
Preterm infants
Term infant whose head rested on the maternal pelvic brim
Maternal/fetal vitamin D deficiency
Syphilis
Extra-cranial collections
Features | Caput | Cephalhematoma | Subgaleal Hematoma |
Location | Crosses suture lines | Distinct margins Do not suture lines | Crosses suture lines “FOOTBALL helmet like “ |
Findings | Firm edema vaguely demarcated | Initially firm, Fluctuant after 48 hours | Diffuse fluid like swelling, shifts to dependent areas , |
Timing | Noted at birth | Hour-days after birth | At birth or hours later |
Volume of blood | None to very little | 10-40ml | 50-100ml |
Scalp defects
Encephalocele
Anencephaly
Cutis Aplasia
Face
Symmetry
Dysmorphism)
Symmetry of Face
Facial palsy
Asymmetric crying face
Mouth��Ebstein Pearls Neonatal Tooth Cleft Palate
Patau- Trisomy 13
Down- Trisomy 21
Edward- Trisomy 18
Beckwith Wiedemann syndrome
Congenital Hypothyroidism
Craniofacial Syndromes
Apert syndrome
prematurely fused facial deformities hypertelorism (wide eyes) and syndactyly
Crouzon syndrome
premature fusion sutures, deformities of mid-face, vision ,hearing ,cleft lip or palate ,no hand or foot deformity
Compound Craniosynostosis
Pfeiffer syndrome:
hypertelorism, hearing loss, dental abnormalities, brachydactyly (short fingers and toes) and syndactyly
Carpenter Syndrome
malformations of hands and feet, cardiovascular deformities, skeletal abnormalities, obesity, vision problems, mental retardation
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