| Description | Match: |
Healthy infant with subcutaneous nodules. Histology shows lymphocytes, histiocytes, giant cells, needle-shaped clefts, fat necrosis, calcification. Hypercalcemia upon resolution.  | Subcutaneous Fat Necrosis of the Newborn |
 | Aplasia Cutis Congenita (ACC) |
 | Acute Hemorrhagic Edema of Infancy (Finkelstein Disease) |
 | Bohn Nodule |
Infant with Hirschprung's  | Jacquet's Erosive Dermatitis |
| Etiology of hand, foot and mouth disease | Coxsackie A16 |
 | Erythema Infectiosum / Fifth Disease (Parvovirus B19) |
| Leading cause of acquired heart disease in children | Kawasaki's disease |
 | Gianotti-Crosti Syndrome (avoid steroid creams) |
Child with Rubella  | Forschheimer Spots |
Genetic defect?  | Peutz-Jeghers Syndrome (STK11 / LKB1) |
 | Nevus Spilus / Speckled Lentiginous Nevus |
This finding along with macrocephaly, lipomas and hemangiomas  | Bannayan-Riley Ruvalcaba |
VBR1 gene, nasal alar hypoplasia, hypothyroidism, congenital deafness, pancreatic achylia  | Johanson-Blizzard Syndrome |
Keratin 14 mutation, palmoplantar hypohidrosis, hyperkeratoses, poor dentition, no dermatoglyphics.  | Naegeli-Franceschetti-Jadassohn |
| What malignancy is associated with NF-1 and multiple Juvenile Xanthogranulomas? | CML |
Positive Darier's Sign. What is the mutated receptor?  | C-Kit (CD 117) |
 | Dermoid Cyst |
 | Infantile Digital Fibroma |
Oral mucosal and gingival lesions, alveolar bone loss, and this finding:  | Floating teeth, Langerhans Cell Histiocytoses |
 | Lymphangioma Circumscriptum |
s/p parotid surgery:  | Auriculotemporal Syndrome (Frey's Syndrome) |
| Livedo reticularis, CVAs, antiphospholipid antibodies | Sneddon Syndrome |
FLTA gene, autosomal dominant lymphedema  | Milroy's Disease |
RASA1 mutation, multiple fast-flow AVMs and limb hypertrophy  | Parkes-Weber Syndrome |
