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  3. Research By Disease

Disease: Merlob syndrome

  • Autosomal dominant isolated question mark ear
  • Correspondence concerning Hunter and Yotsuyanagi's "the external ear: more attention to detail may aid syndrome and contribute answers to embryological questions"
  • Gastroschisis and associated defects: an international study
  • In utero oxcarbazepine and a withdrawal syndrome, anomalies, and hyponatremia
  • Leptin, insulin, insulin-like growth factors and their binding proteins in cord serum: insight into fetal growth and discordancy
  • Long-term outcome following selective serotonin reuptake inhibitor induced neonatal abstinence syndrome
  • Mortality of full-term infants during the first month of life in a tertiary care hospital
  • Neonatal abstinence syndrome after in utero exposure to selective serotonin reuptake inhibitors in term infants
  • New syndrome of congenital circumferential skin folds associated with multiple congenital anomalies
  • Outcome of infants exposed to olanzapine during breastfeeding
  • Poland sequence with bilateral features: a suggestion
  • Pregnancy outcome following maternal exposure to pregabalin may call for concern
  • Prevalence at birth of cleft lip with or without cleft palate: data from the International Perinatal Database of Typical Oral Clefts (IPDTOC)
  • Selective serotonin reuptake inhibitor induced neonatal abstinence syndrome
  • Yunis-Varon syndrome: further delineation of the phenotype
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CheckOrphan is a non-profit organization located in Basel, Switzerland and Santa Cruz, California that is dedicated to rare, orphan and neglected diseases. CheckOrphan offers users an interactive and dynamic platform for all these diseases. This strategy allows visitors to be updated daily on all the latest news and interact with people internationally. This is essential, because due to the nature of these diseases, there is not a large concentration of individuals within any given proximity.
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