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Dystrophic epidermolysis bullosa is a rare, chronic non-inflammatory bullous disease, which easily forms bullae by minor mechanical trauma or spontaneously, is inherited either in an autosomal dominant or autosomal recessive fashion. We report herein two cases which presented with bullae, erosions and ulcers on extremities, buttock, chest, abdomen and face and loss of all nail since birth in two sisters. Bulla occured bencath the basal lamina histopathologically, anchoring fibrils were almost absent on electron miaoscopy in both cases. The two sisters represented dystrophic epidermolysis bullosa considering the absence of family history inheritcd in an autosomal dominant fashion and the clinical, histological and electronmicroscopic findings.
Abdomen ; Basement Membrane ; Buttocks ; Epidermolysis Bullosa Dystrophica* ; Extremities ; Humans ; Parturition ; Siblings* ; Thorax ; Ulcer

10.Whole Cow's milk Related iron Deficiency Anemia in Early Childhood.

In Sang JEON ; Heon Seok HAN ; Hyo Seop AHN ; Jin Q KIM

Journal of the Korean Pediatric Society 1990;33(10):1374-1379

1.A Case of Bilateral Wilms' Tumor.

2.A clinical study on Myasthenia gravis in childhood.

3.A Clinical Study of Childhood Non-Hodgkin's Lymphoma.

4.A clinical study on histiocytosis X.

5.Study on the treatment of childhood acute lymphoblastic leukemia.

6.Fanconi Anemia.

7.A case of pancytopenia associated with mycoplasmal pneumonia.

8.Clinical Obseervation for Hematologic Disorders in Children.

9.Dystrophic Epidermolysis Bullosa in Two Sisters.

10.Whole Cow's milk Related iron Deficiency Anemia in Early Childhood.

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