Distinctive pitted enamel hypoplasia and short stature
We report a case of postnatal onset short stature and a distinctive pitted enamel hypoplasia in a 19-year-old woman. Growth hormone deficiency and other endocrine deficiencies were excluded. Additional observations of similar cases might outline a newly recognized syndrome.
Saved in:
| Main Authors: | , , |
|---|---|
| Format: | Article (Journal) |
| Language: | English |
| Published: |
2000
|
| In: |
Journal of craniofacial genetics and developmental biology
Year: 2000, Volume: 20, Issue: 3, Pages: 155-156 |
| ISSN: | 0270-4145 |
| Online Access: |
|
| Author Notes: | M.J. Koch, S. Spranger, M. Bettendorf |
| Summary: | We report a case of postnatal onset short stature and a distinctive pitted enamel hypoplasia in a 19-year-old woman. Growth hormone deficiency and other endocrine deficiencies were excluded. Additional observations of similar cases might outline a newly recognized syndrome. |
|---|---|
| ISSN: | 0270-4145 |