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.

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Bibliographische Detailangaben
Hauptverfasser: Koch, Martin Jean (Verfasst von) , Spranger, Stephanie (Verfasst von) , Bettendorf, Markus (Verfasst von)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: 2000
In: Journal of craniofacial genetics and developmental biology
Year: 2000, Jahrgang: 20, Heft: 3, Pages: 155-156
ISSN:0270-4145
Online-Zugang: Volltext
Verfasserangaben:M.J. Koch, S. Spranger, M. Bettendorf
Beschreibung
Zusammenfassung: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