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Identifying & Managing Skull Deformities in Pediatrics: Plagiocephaly & Craniosynostosis, Slides of Pediatrics

An in-depth analysis of skull deformities in pediatrics, focusing on plagiocephaly and craniosynostosis. It includes case studies, normal and abnormal skull growth patterns, risk factors, diagnosis, treatment, and referral guidelines. Useful for medical students, nurses, and healthcare professionals.

Typology: Slides

2012/2013

Uploaded on 10/01/2013

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Download Identifying & Managing Skull Deformities in Pediatrics: Plagiocephaly & Craniosynostosis and more Slides Pediatrics in PDF only on Docsity!

Skull Deformities

in Pediatrics

Case 1

 7wk female with parental concern over

head shape

 PMHx:

 35wk twin A; NICU x 6days (FEN, ID, bili)  Normal feeding/wets/stools  Progressive “flattening” of head since birth  No hx IVH; no neurological symptoms  No flattening in twin

What’s normal?

Skull growth mainly secondary to brain growth  40% adult size at term  90% adult size by 1yo  95% adult size by 6yo  Suture closure  PF 3-6mo  AF 9-18mo  C,S,L sutures 40years

What’s most likely?

 Deformational Plagiocephaly:

 Asymmetric head  Up to 48% healthy infants  Most common referral to Peds NSGY

 Risk Factors:  Intrauterine crowding/positioning  Decreased mobility (dev.delay, MR, prematurity)  Posturing (torticollis, C-spine defect)  “Back to Sleep” campaign  Increased physician awareness

What’s a Pediatrician to do? The H&P, of course!

 Molding

 Pressure in AP dimension (labor)  Resolves in hours-weeks

 Deformation

 Pressure in local region (occipital)  No sutural ridging; bones mobile

 Synostosis

 Premature closure of sutures  Palpable ridges over suture; bones immobile

What’s normal?

Deformational Plagiocephaly Lambdoid Synostosis

PARALLELOGRAM TRAPEZOID

What’s not?

Sagittal Synostosis

Deformational Plagiocephaly

 AKA: Positional, Posterior, Occipital,

Plagiocephaly without synostosis

 Diagnosis:

 Usually clear based on H&P  Head shape (parallelogram)  Xray if unsure – sutures patent

When to refer?

 True craniosynostosis

 1/5-1/6 syndromic  Increased risk ICP, hydrocephalus, Chiari

 Multi-D Team:

 NSGY, Plastics, Ophtho, Neuro, ENT, Orthodontics, Psych, Genetics, Social Work

 Neurosurgery: 3-9 months old

Case 2

 Newborn female, term SVD

 No maternal hx; no family hx

 Physical Exam:

 Large, low AF  ?Fused coronal/lambdoid sutures?  Significant caput  Hypertelorism  Syndactyly on 3 extremities; clubfoot  Broad, flat hallux