796 results
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings
Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
in utero as the placenta ... pathophysiology #genetics ... endocrinology #peds
Placental Abruption 
Premature separation of the implanted placenta from the uterine wall 
PAINFUL vaginal bleeding but..
Placental Abruption ... the implanted placenta ... internal) #Placental
Causes of Late Bleeding in Pregnancy (2nd & 3rd Trimester) - Differential Diagnosis Algorithm
Bleeding from Os
- Painful: • Placental ... Painless: • Placenta
Causes of Intrauterine Growth Restriction / Small for Gestational Age - Differential Diagnosis Algorithm
Fetal Factors:
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syndrome, 45X Placental ... Factors: - Placental ... Infarction • Placenta ... insufficiency - Placental ... Abruption - Placental
Prader-Willi Syndrome: Pathogenesis and clinical findings
 • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
chromosome ->Loss of parental ... PraderWilli #Syndrome #genetics ... pathophysiology #peds
Embryonic and Placental Development

#Embryonic #Placental #Development #Implantation #Obstetrics #Embryology
Embryonic and Placental ... #Embryonic #Placental
Role of G6PD in Protection against Oxidative Damage #Pathophys #Peds #Genetics #Honc #Favism #g6pd #NEJM
Damage #Pathophys #Peds ... #Genetics #Honc
Harlequin Ichthyosis

Rare genetic disorder that results in thickened skin over nearly the entire surface of the
Ichthyosis Rare genetic ... physicalexam #pediatrics #genetics
Placental Locations 
#Ultrasound #OBGYN #Placenta
Placental Locations ... Ultrasound #OBGYN #Placenta
Metabolism of plasma lipoproteins and related genetic diseases - Familial Hypercholesterolemia
Type I (FAMILIAL HYPERCHYLOMICRONEMIA) 
Type IIA
lipoproteins and related genetic ... #lipoproteins #genetics