Endocrinology · Endocrinology / Bone and mineral disorders
Sanjad–Sakati syndrome
also: Hypoparathyroidism, retardation and dysmorphism
Recessive hypoparathyroidism with growth failure and dysmorphism.
- Specialty
- Endocrinology
- Subspecialty
- Endocrinology / Bone and mineral disorders
- Sex & age distribution
- Male: affected; Female: affected equally; Children: yes, Arab populations
- Gene(s) involved
- TBCE
- Alternative names & eponyms
- Hypoparathyroidism, retardation and dysmorphism
Etiology & mechanism
TBCE variants.
Gene(s) involved (1)
Symptoms & signs (6)
In plain terms, someone with Sanjad–Sakati syndrome may experience the following — click any to explore related syndromes:
Same gene(s)
Other syndromes that involve one of this syndrome's genes.
Overlapping symptoms
Other syndromes that share symptoms with this one.
Drag nodes, scroll to zoom, click a node to open that syndrome.
Shares symptoms with
2 shared
Angelman syndrome
microcephaly, seizures
2 shared
Barakat syndrome
hypocalcemia, seizures
2 shared
Borjeson–Forssman–Lehmann syndrome
intellectual disability, seizures
2 shared
Cardiofaciocutaneous syndrome
intellectual disability, seizures
2 shared
Cerebral folate deficiency syndrome
microcephaly, seizures
2 shared
Cockayne syndrome
growth failure, microcephaly
2 shared
Cohen syndrome
intellectual disability, microcephaly
2 shared
Congenital Zika syndrome
microcephaly, seizures
2 shared
Cornelia de Lange syndrome
growth failure, intellectual disability
2 shared
Cri du chat syndrome
intellectual disability, microcephaly
Shares genes with
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