Microphthalmia, Lenz type (Q94949): Difference between revisions
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Microftalmia tipo Lenz é uma forma sindrômica de microftalmia caracterizada por coloboma, microftalmia e catarata, associada a anormalidades esqueléticas e/ou digitais que afetam as clavículas e polegares (clinodactilia), déficit intelectual e transtornos de crescimento, microcefalia, orelhas descoladas, palato oco e dentário anormalidades, hipoplasia renal, criptorquidia e cardiopatia congênita. | |||
| description / en | description / en | ||
Microphthalmia, Lenz type is a syndromic form of microphthalmia characterised by coloboma, microphthalmia and cataract, associated with skeletal and/or digital abnormalities affecting the clavicles and thumbs (clinodactily), intellectual deficit and growth disorders, microcephaly, detached ears, hollow palate and dental abnormalities, renal hypoplasia, cryptorchidism, and congenital cardiopathy. | |||
Revision as of 10:30, 16 August 2026
Microphthalmia, Lenz type is a syndromic form of microphthalmia characterised by coloboma, microphthalmia and cataract, associated with skeletal and/or digital abnormalities affecting the clavicles and thumbs (clinodactily), intellectual deficit and growth disorders, microcephaly, detached ears, hollow palate and dental abnormalities, renal hypoplasia, cryptorchidism, and congenital cardiopathy.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_678242327 |
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| English | Microphthalmia, Lenz type |
Microphthalmia, Lenz type is a syndromic form of microphthalmia characterised by coloboma, microphthalmia and cataract, associated with skeletal and/or digital abnormalities affecting the clavicles and thumbs (clinodactily), intellectual deficit and growth disorders, microcephaly, detached ears, hollow palate and dental abnormalities, renal hypoplasia, cryptorchidism, and congenital cardiopathy. |
