Lujan syndrome in a Mexican boy
✍ Scribed by Rivera, H. ;Ramírez-Dueñas, M. L. ;García-Ochoa, C.
- Publisher
- John Wiley and Sons
- Year
- 1992
- Tongue
- English
- Weight
- 151 KB
- Volume
- 43
- Category
- Article
- ISSN
- 0148-7299
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
We present a patient and his maternal uncle who have a subaortic ventricular septal defect and aortic root dilation. They both have physical anomalies, characteristic behaviors, and cognitive disabilities that are consistent with the diagnosis of Lujan-Fryns syndrome (LFS). Although there have been
Schizophrenia is considered to be a heterogenous disorder. Different etiopathological mechanisms can be attributed to a similar clinical picture as described in DSM-111-R criteria. We present a case of a young man diagnosed on different occasions as schizophrenic with mild mental retardation. Clinic
CHILD syndrome (congenital hemidysplasia with ichthyosiform nevus and limb defects) occurs, as a rule, exclusively in girls because the underlying X-linked gene exerts a lethal effect on male embryos. In this report the characteristic manifestations of CHILD syndrome are described in a 2-yearold boy