IAP MADURAI : PEDIATRIC ACADEMIC MEET (30th April 2021)
11 replies on “IAP MADURAI : PEDIATRIC ACADEMIC MEET (30th April 2021)”
Should anticoagulant be given to a child presenting with neurological manifestation with acute covid
Excellent cases and fabulous presentations. Congratulations
Very informative presentation on neurological manifestations of covid
What are the possible causes of sudden seizures and unresponsive mess D 5 of illness with rt pcr positive in 13 year old boy…we had a case
Sex steroids from ovaries will determine puberty. So, absence of reticularis will affect adrenarche; but not the true puberty.
Wonderful presentation of rare case of Glucocorticoid deficiency !
Disuse atrophy is seen in stroke. Similarly, ACTH stimulates growth of zona glomerulosa and fasciculata – so they are atrophied
No an steroids tried so far
Clinical features of any syndrome gradually evolve over time
Arthrogryposis multiplex with thymic hyperplasia
Could this baby have common mutation causing the skeletal abnormality and thymic hyperplasia –
Could this be an earl manifestation of Loeys Dietz syndrome like illness
DIAP India
11 replies on “IAP MADURAI : PEDIATRIC ACADEMIC MEET (30th April 2021)”
Should anticoagulant be given to a child presenting with neurological manifestation with acute covid
Excellent cases and fabulous presentations. Congratulations
Very informative presentation on neurological manifestations of covid
What are the possible causes of sudden seizures and unresponsive mess D 5 of illness with rt pcr positive in 13 year old boy…we had a case
Sex steroids from ovaries will determine puberty. So, absence of reticularis will affect adrenarche; but not the true puberty.
Wonderful presentation of rare case of Glucocorticoid deficiency !
Disuse atrophy is seen in stroke. Similarly, ACTH stimulates growth of zona glomerulosa and fasciculata – so they are atrophied
No an steroids tried so far
Clinical features of any syndrome gradually evolve over time
Arthrogryposis multiplex with thymic hyperplasia
Could this baby have common mutation causing the skeletal abnormality and thymic hyperplasia –
Could this be an earl manifestation of Loeys Dietz syndrome like illness