Kindler syndrome in Infant/Neonate
KS is inherited in an autosomal recessive pattern that results from a loss-of-function in the FERMT1 gene (formerly KIND1), which encodes a protein known as fermitin family homolog 1 (FFH1), a focal adhesion protein that links the actin cytoskeleton with the underlying extra cellular matrix. Weakness at this point causes splits at various levels, most often above the basal keratinocytes.
Like other forms of EB, blisters in KS are typically noted soon after birth or in early infancy; there is a predilection for acral sites. Disease severity may range from mild, with minimal skin disease, to severe with involvement of mucosal sites (such as conjunctiva, vagina, urethra, anus, and mouth) and gastrointestinal tract (causing esophageal strictures and colitis). Patients with mild disease may not be diagnosed until late in adulthood.
Features that distinguish KS from other types of EB are photosensitivity, progressive poikiloderma, and marked skin atrophy, which begin early in the disease course. While blistering and photosensitivity tend to diminish in severity with age, poikiloderma is permanent. Scarring is usually minimal, but repeated trauma can result in development of scar tissue.
Other clinical findings of KS include hyperkeratosis of the palms and soles, joint laxity, severe periodontal disease, ectropion, webbing of the fingers and toes, nail dystrophy, esophageal and urethral stenosis, and phimosis, although these findings are typically sequelae seen later in childhood or adulthood.
With the increased photosensitivity, there is also an increased risk of nonmelanoma skin cancer in KS, with squamous cell carcinomas (SCC) reported in acral skin and the mouth.
For more information, see OMIM.
Related topics: EB simplex, generalized severe EB simplex, junctional EB, dystrophic EB, EB acquisita
Q81.8 – Other epidermolysis bullosa
238836000 – Kindler syndrome
- Other forms of EB including dystrophic EB and EB simplex, specifically the skin mottling subtype
- Photosensitive porphyrias – eg, erythropoietic protoporphyria (EPP), congenital erythropoietic porphyria (CEP), porphyria cutanea tarda (PCT), variegate porphyria
- Dyskeratosis congenita
- Incontinentia pigmenti
- Bloom syndrome
- Rothmund-Thomson syndrome
- Xeroderma pigmentosum
- Bullous mastocytosis
- Acrodermatitis enteropathica
- Neonatal herpes simplex virus
- Bullous impetigo
- Stevens-Johnson syndrome