Gamuts

Cranioectodermal dysplasia

Sensenbrenner syndrome (OMIM #218330) is a rare (less than 20 cases reported by 2010) multisystem disease first described by Judith A. Sensenbrenner in 1975. It is inherited in an autosomal recessive fashion, and a number of genes appear to be responsible. [Source: Wikipedia ]

OrphaNet reference
Cranioectodermal dysplasia 
Subtypes
Cranioectodermal dysplasia type 1
Cranioectodermal dysplasia type 2
May Cause
Agenesis or hypoplasia of the corpus callosum
Alopecia
Anodontia or hypodontia
Brachydactyly
Clinodactyly
Congenital generalized osteoporosis
Congenital macrocephaly
Craniosynostosis
Defective dentition
Delayed dentition
Dental defect
Ectodermal dysplasia
Hypertelorism
Macrocephaly
Microdontia
Myopia
Nystagmus
Round vertebrae
OrphaNet reference
Cranioectodermal dysplasia 
Subtypes
Cranioectodermal dysplasia type 1
Cranioectodermal dysplasia type 2
May Cause
Agenesis or hypoplasia of the corpus callosum
Alopecia
Anodontia or hypodontia
Brachydactyly
Clinodactyly
Congenital generalized osteoporosis
Congenital macrocephaly
Craniosynostosis
Defective dentition
Delayed dentition
Dental defect
Ectodermal dysplasia
Hypertelorism
Macrocephaly
Microdontia
Myopia
Nystagmus
Round vertebrae


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