Hypoparathyroidism- retardation- dysmorphism syndrome

Hypoparathyroidism short stature mental retardation seizures retardation, and developmental delay
Also Known As:
Hypoparathyroidism with short stature, mental retardation, and seizures; Sanjad-Sakati syndrome
Networked: 18 relevant articles (0 outcomes, 0 trials/studies)

Bio-Agent Context: Research Results


1. Pal, Kamalesh: 2 articles (05/2010 - 02/2010)
2. Parvari, Ruti: 2 articles (03/2006 - 11/2002)
3. Sakka, R: 1 article (09/2015)
4. Ben Ameur, K: 1 article (09/2015)
5. Ben Hmida, H: 1 article (09/2015)
6. Sfar, S: 1 article (09/2015)
7. Ghédira, E S: 1 article (09/2015)
8. Monastiri, K: 1 article (09/2015)
9. Kerkeni, E: 1 article (09/2015)
10. Ghedira, N: 1 article (09/2015)

Related Diseases

1. Hypoparathyroidism
2. Mental Retardation (Idiocy)
3. Seizures (Seizure)
03/15/2006 - "Hypoparathyroidism-retardation-dysmorphism (HRD) or Sanjad-Sakati syndrome (SSS) (OMIM 241410) is a rare autosomal recessive (AR) inherited condition, characterized by congenital hypoparathyroidism (hypoPTH), retardation, seizures, and a typical facial dysmorphism, consisting of prominent forehead, deep-set eyes, and abnormal external ears. "
09/01/2015 - "Sanjad-Sakati syndrome (SSS) (OMIM 241410) is a rare autosomal recessive disorder characterized by congenital hypoparathyroidism with growth and mental retardation associated with seizures and a characteristic physiognomy. "
07/02/1999 - "The Sanjad-Sakati syndrome (SSS; MIM241410), an autosomal recessive trait characterized by congenital hypoparathyroidism, growth and mental retardation, seizures, and a characteristic physiognomy, was recently linked to chromosome area 1q42-q43. "
06/01/2010 - "Sanjad--Sakati syndrome (SSS) is a genetic disease confined to Arab populations in the Middle- East countries and characterized by hypoparathyroidism, hypocalcaemia and hyperphosphataemia, severe intrauterine and postnatal growth failure, respiratory infection susceptibility prone, dwarfism, mental retardation, seizures, craniofacial dysmorphic features as retromicrognathia and abnormal dentition. "
11/01/2006 - "Sanjad-Sakati syndrome (SSS) is a rare genetic disorder characterized by congenital hypoparathyroidism, hypocalcemia and hyperphosphatemia, seizures, severe intrauterine and postnatal growth failure, dwarfism, mental retardation, dysmorphic features including retromicrognathia and abnormal dentition and increased susceptibility to infection. "
4. Infection
5. Dwarfism

Related Drugs and Biologics

1. Kenny Caffey syndrome
2. Tubulin