Cranioectodermal dysplasia: A new patient with an inapparent, subtle phenotype

Pediatric Dermatology

Volumn 18, Issue 4, 2001, Pages 332-335

  Zannolli, R ^a   Mostardini, R ^a   Carpentieri, M L ^a   Gatti, M G ^a   Galluzzi, P ^a   Terrosi Vagnoli, P ^a   Giorgetti, R ^a   Calvieri, S ^b   Morgese, G ^c  

^a UNIVERSITY OF SIENA   (Italy)

^b UNIVERSITY HOSPITAL OF SIENA   (Italy)

^c SAPIENZA UNIVERSITY OF ROME   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CASE REPORT; CLINODACTYLY; CORPUS CALLOSUM; CRANIOECTODERMAL DYSPLASIA; ECTODERMAL DYSPLASIA; FEMALE; HUMAN; HYPERMETROPIA; HYPERTELORISM; KIDNEY FAILURE; PHENOTYPE; PRESCHOOL CHILD; PRIORITY JOURNAL; SKELETON MALFORMATION; SKULL MALFORMATION; SYNDROME;

BONE AND BONES; CHILD, PRESCHOOL; CRANIOFACIAL ABNORMALITIES; ECTODERMAL DYSPLASIA; FEMALE; FOLLOW-UP STUDIES; HAIR; HAND DEFORMITIES, CONGENITAL; HUMANS; ITALY; MAGNETIC RESONANCE IMAGING; PHENOTYPE; SYNDROME; TOOTH ABNORMALITIES;

EID: 0034856028     PISSN: 07368046     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1525-1470.2001.01955.x     Document Type: Article

References (10)

1. New syndrome of skeletal, dental and hair anomalies
2. A heritable syndrome of craniosynostosis, short thin hair, dental abnormalities, and short limbs: Cranioectodermal dysplasia
3. Neurologic abnormalities in the skeletal dysplasias: A clinical and radiological perspective
4. Ectodermal dysplasias: A clinical classification and a causal review
5. A new oculorenal syndrome: Retinal dystrophy and tubulointerstitial nephropathy in cranioectodermal dysplasia
6. Chronic tubulo-interstitial nephropathy in children with cranioectodermal dysplasia
7. Chronic renal failure and cranioectodermal dysplasia: A further step
8. Expanded phenotype of cranioectodermal dysplasia
9. Phenotype of cranioectodermal dysplasia with different hair and bone abnormalities