Atopic dermatitis
Atopic dermatitis (AD) is a chronic, relapsing, pruritic inflammatory skin disease that occurs most frequently in children. more… Atopic dermatitis
Open-Source Dermatology Education Resources
Atopic dermatitis (AD) is a chronic, relapsing, pruritic inflammatory skin disease that occurs most frequently in children. more… Atopic dermatitis
Café-au-lait macules (CALMs) are flat, hyperpigmented, irregularly shaped skin lesions (macules or patches) that may be present at birth and may grow in number and size. Stemming from the French language, CALMs get their unique name from their typical coloring, which resembles “coffee with milk.” more… Café au lait spot
Transient neonatal pustular melanosis (TNPM) is a rare benign vesiculopustular eruption seen in all ethnic groups, but mostly in full-term dark-skinned infants. more… Transient neonatal pustular melanosis
Infantile hemangiomas are common benign vascular tumors that affect infants. The lesion usually presents shortly after birth and can appear anywhere on the body, with up to 50% appearing on the head and neck. more… Infantile Hemangioma
Roseola infantum isacommon viral exanthem of childhood. Itis characterized by afever followed by a rashupon defervescence.It is typicallycaused by infection with human herpesvirus (HHV) type 6 or 7. more… Roseola Infantum
Scarlet fever is a clinical syndrome caused by certain strains of Group A streptococcal (GAS) bacteria that release the streptococcal pyrogenic exotoxin. more… Scarlet fever
Seborrheic dermatitis (SD) is a common inflammatory skin condition that is chronic and relapsing. more… Seborrheic dermatitis
Sturge-Weber Syndrome (SWS) is a rare, sporadic neurocutaneous disorder characterized by the hallmark triad of a facial port-wine stain, leptomeningeal angiomatosis, and ocular vascular anomalies. more… Sturge-Weber syndrome
Tuberous sclerosis complex (TSC) is a genetic syndrome with multiorgan involvement including brain, skin, kidneys, heart, eyes, and lung. TSC is characterized by hamartomas, or abnormal growth of normal tissues. more… Tuberous sclerosis
Xeroderma pigmentosum (XP) is a rare genodermatosis characterized by defective DNA repair and inherited in an autosomal recessive fashion. more… Xeroderma pigmentosa