[On eye changes associated with the pigmented spots syndrome (Peutz-Jeghers) (author's transl)]

Autor:	H, Rieger, H, Dibold
Jazyk:	němčina
Rok vydání:	1978
Předmět:	Eye Diseases Peutz-Jeghers Syndrome Humans Female Middle Aged Pedigree
Zdroj:	Klinische Monatsblatter fur Augenheilkunde. 173(6)
ISSN:	0023-2165
Popis:	After a survey of cases of the pigmentpolyposis (Peutz-Jeghers) in the literature reported, a woman with an abortive form of this syndrome (pigmentanomaly ) and a bilateral embryotoxon posterius (Axenfeld) is described. Both signs are heritable in the autosomal-dominant manner. The association of pigmentpolyposis and embryotoxon is not yet observed. Possibly there is present a new-mutation. The examination of the family detected no other special cases. For the future on had in cases of pigmentpolyposis possible ocular changes more in view than till now.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=pmid________::5d83ff84d241ca25fcb05cef14fb387d https://pubmed.ncbi.nlm.nih.gov/732203 Zobrazit plný text záznamu