Zamzam–Sheriff–Phillips syndrome
| Zamzam–Sheriff–Phillips syndrome | |
|---|---|
| Synonyms | ZSPS |
| Pronounce | N/A |
| Specialty | Medical genetics |
| Symptoms | Intellectual disability, short stature, microcephaly, facial dysmorphism, skeletal abnormalities |
| Complications | N/A |
| Onset | Congenital |
| Duration | Lifelong |
| Types | N/A |
| Causes | Genetic mutation |
| Risks | Family history |
| Diagnosis | Clinical evaluation, genetic testing |
| Differential diagnosis | Other genetic syndromes |
| Prevention | N/A |
| Treatment | Supportive care, symptomatic treatment |
| Medication | N/A |
| Prognosis | Variable |
| Frequency | Extremely rare |
| Deaths | N/A |
Zamzam-Sheriff-Phillips syndrome is a rare autosomal recessive congenital disorder. It is characterized by aniridia, ectopia lentis, abnormal upper incisors and intellectual disability. Not a lot of research has been undertaken of this particular disease so thus far there is no known gene that affects this condition. However it has been hypothesised that the symptoms described are found at a particular gene, though intellectual disability is believed to be due to a different genetic cause. Consanguinuity (intermarrying among relatives such as cousins), often associated with autosomal recessive inheritance, has been attributed to the inheritance of this disease.[1]
References[edit]
- ↑ "Aniridia, ectopia lentis, abnormal upper incisors and mental retardation--an autosomal recessive syndrome".Jpn. J. Ophthalmol..1988;32(4)
- 375–8.PMID:3266265.
| Congenital malformations and deformations of eyes | ||||
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