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.
Gespeichert in:
| Hauptverfasser: | , , |
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| Dokumenttyp: | Article (Journal) |
| Sprache: | Englisch |
| Veröffentlicht: |
2000
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| In: |
Journal of craniofacial genetics and developmental biology
Year: 2000, Jahrgang: 20, Heft: 3, Pages: 155-156 |
| ISSN: | 0270-4145 |
| Online-Zugang: |
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| Verfasserangaben: | M.J. Koch, S. Spranger, M. Bettendorf |
MARC
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| 520 | |a 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. | ||
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