Features of this genetic condition include:
- micrognathia, abnormal external ears, clenched hands with overlapping fingers, increased muscle tone, low birth weight, single umbilical artery, short palpebral fissures, nail hypoplasia, and congenital heart defects (ventricular septal defect, atrial septal defect, and patent ductus arteriosus)
Trisomy 18
sloping forehead with holoprosencephaly, microphthalmia, cleft lip or palate, and polydactyly
Trisomy 13
Hemangioma involution
50% by 5 years
70% by 7 years
90% by 9 years
GLUT-1 positive
Hemangiomas
Kasabach-Meritt (KHE, Tufted Angioma)
- GI, Pulmonary, CNS, Liver Angiomas
Neonatal Hemangiomatosis
PHACES Syndrome
SWS
Lumbosacral hemangiomas
Tethered cord, intraspinal lipomas
Liver hemangiomas
HM, CHF, anemia and thrombocytopenia
Hypothyroidism
Salmon Patch
- Grows with the child, darkens with age, becomes cobblestoned with soft tissue hypertrophy
Port Wine Stains (Nevus flammeus)
Rx: Pulse Dye Laser
Klippel Trenaunay
Pyogenic Granuloma (Lobular Capillary Hemangioma)
- Dome-shaped, red to yellow to brown color
Spitz Nevus
- Very low risk of malignancy, but a malignant melanoma can mimic a spitz nevus
Erythema Toxicum
Transient Neonatal Pustular Melanosis
Normal mottled response to cold
Cutis Marmorata
Cutis Marmorata Telangiectatica Congenita
Subcutaneous Fat Necrosis
Neonatal Acne
Acne that has a later onset or is prolonged, may be severe and require evaluation of androgens, Infantile acne
Dermatitis on interdigital/arch of foot
Tinea pedis
Dermatitis on weight-bearing surface of foot
Juvenile Plantar Dermatosis
Dermatitis on dorsum of foot
Contact dermatitis