A 2-week-old neonate born enclosed in a transparent, glistening, collodion-like sac presented with generalized erythema with shiny, tight, fissured skin allover the body with some degree of ectropion and eclabium.

          A 21-year-old male presented with increasing number of bilateral symmetrical flesh-colored to brownish discrete waxy translucent papules involved the nose and cheeks. The lesions started to appear since age of 4-5 years. He had no other cutaneous or systemic manifestation of tuberous sclerosis.

          A 7-year-old boy presented with an asymptomatic, bilateral symmetrical cirbriform (honeycomb) atrophy of the cheeks since birth. There was no associated heart or neurological disease.

          Multiple, asymptomatic, rounded, circular (ring-like),  atrophic plaques confined to one cheek have been noticed since birth in a one-year-old male infant.

          A 5-year-old girl presented with multiple, asymptomatic, skin-colored firm papules involving the cheeks and nose since age of two years. Child’s mentality was subnormal, however, till time of presentation there were no other associated features of tuberous sclerosis complex.

       A unilateral congenital semicircular to oval brown patch with well-defined irregular border on the anterior aspect of the elbow region of a 4-year-old girl.

           A 2-year-old female child presented with a congenital, oval, atrophic, hypopigmented patch with slightly hyperpigmented border on the anterior aspect of the neck. There was no similar family history or preceding skin disease.

           An asymptomatic, oval-shaped brownish patch involved the forhead since birth in a 16-year-old female.