McDonough syndrome (Q94183): Difference between revisions
From determinar.ia.br - Determine suas informações
Created a new Item |
Changed label, description and/or aliases in pt-br, en |
||
| description / pt-br | description / pt-br | ||
A síndrome de McDonough pertence ao grupo de síndromes de anomalias congênitas múltiplas/incapacidade intelectual (MCA/MR) e é caracterizada por déficit intelectual, fácies distintiva (fissuras palpebrais inclinadas para cima, estrabismo), cifoescoliose, diástase dos retos abdominais, criptorquidia e um defeito cardíaco congênito. | |||
| description / en | description / en | ||
McDonough syndrome belongs to the group of multiple congenital anomalies/mental retardation (MCA/MR) syndromes and is characterised by intellectual deficit, distinctive facies (upward slanting palpebral fissures, squint), kyphoscoliosis, diastasis recti, cryptorchidism, and a congenital heart defect. | |||
Revision as of 09:18, 16 August 2026
McDonough syndrome belongs to the group of multiple congenital anomalies/mental retardation (MCA/MR) syndromes and is characterised by intellectual deficit, distinctive facies (upward slanting palpebral fissures, squint), kyphoscoliosis, diastasis recti, cryptorchidism, and a congenital heart defect.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1349711155 |
||
| English | McDonough syndrome |
McDonough syndrome belongs to the group of multiple congenital anomalies/mental retardation (MCA/MR) syndromes and is characterised by intellectual deficit, distinctive facies (upward slanting palpebral fissures, squint), kyphoscoliosis, diastasis recti, cryptorchidism, and a congenital heart defect. |
