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About 234 results

ALLMedicine™ Neonatal Hemochromatosis Center

Research & Reviews  117 results

PIGA Mutations Can Mimic Neonatal Hemochromatosis.
https://doi.org/10.1542/peds.2020-0918
Pediatrics Flores-Torres J, Carver JD et. al.

Feb 26th, 2021 - Neonatal hemochromatosis (NH), one of the most common causes of liver failure in the neonate, often causes fetal loss or death during the neonatal period. Most cases are thought to be due to gestational alloimmune disease; however, other rare caus...

Hemophagocytic lymphohistiocytosis mimicking neonatal hemochromatosis.
https://doi.org/10.1080/08880018.2019.1654051
Pediatric Hematology and Oncology; Broglie L, Vitola B et. al.

Aug 19th, 2019 - Hemophagocytic lymphohistiocytosis (HLH) is a potentially fatal illness characterized by impaired natural killer (NK) cell and cytotoxic T-cell function. Patients develop systemic inflammation, multisystem organ dysfunction, and if untreated, deat...

Sub-acute neonatal hemochromatosis in an infant with hypoplastic left heart syndrome on...
https://doi.org/10.1111/petr.13567
Pediatric Transplantation REFERENCES; Tadros HJ, Gupta D et. al.

Aug 13th, 2019 - Single-ventricle pediatric patients, amongst other children waiting for OHT, are a vulnerable population, especially if candidacy is established before any palliation. NH is a rare disease with poor prognosis in the post-natal period. We present a...

Neonatal hemochromatosis in a newborn with Down syndrome.
https://doi.org/10.1080/15513815.2019.1627630
Fetal and Pediatric Pathology; M R, Purkait S et. al.

Jun 19th, 2019 - Background: Neonatal hemochromatosis (NH) is a cause of neonatal/pediatric acute liver failure. Liver dysfunction/failure in Down syndrome had been described in relation to increased susceptibility to infection and transient myeloproliferative dis...

A case of Niemann-Pick disease type C with neonatal liver failure initially diagnosed a...
https://doi.org/10.1016/j.braindev.2019.01.004
Brain & Development; Kumagai T, Terashima H et. al.

Feb 9th, 2019 - Niemann-Pick type C (NPC) is a lysosomal lipid storage disease with mutation of NPC1/NPC2 genes, which transport lipids in the endosome and lysosome, and various neurological symptoms. NPC patients also develop hepatosplenomegaly or liver disorder...

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Clinicaltrials.gov  117 results

PIGA Mutations Can Mimic Neonatal Hemochromatosis.
https://doi.org/10.1542/peds.2020-0918
Pediatrics Flores-Torres J, Carver JD et. al.

Feb 26th, 2021 - Neonatal hemochromatosis (NH), one of the most common causes of liver failure in the neonate, often causes fetal loss or death during the neonatal period. Most cases are thought to be due to gestational alloimmune disease; however, other rare caus...

Hemophagocytic lymphohistiocytosis mimicking neonatal hemochromatosis.
https://doi.org/10.1080/08880018.2019.1654051
Pediatric Hematology and Oncology; Broglie L, Vitola B et. al.

Aug 19th, 2019 - Hemophagocytic lymphohistiocytosis (HLH) is a potentially fatal illness characterized by impaired natural killer (NK) cell and cytotoxic T-cell function. Patients develop systemic inflammation, multisystem organ dysfunction, and if untreated, deat...

Sub-acute neonatal hemochromatosis in an infant with hypoplastic left heart syndrome on...
https://doi.org/10.1111/petr.13567
Pediatric Transplantation REFERENCES; Tadros HJ, Gupta D et. al.

Aug 13th, 2019 - Single-ventricle pediatric patients, amongst other children waiting for OHT, are a vulnerable population, especially if candidacy is established before any palliation. NH is a rare disease with poor prognosis in the post-natal period. We present a...

Neonatal hemochromatosis in a newborn with Down syndrome.
https://doi.org/10.1080/15513815.2019.1627630
Fetal and Pediatric Pathology; M R, Purkait S et. al.

Jun 19th, 2019 - Background: Neonatal hemochromatosis (NH) is a cause of neonatal/pediatric acute liver failure. Liver dysfunction/failure in Down syndrome had been described in relation to increased susceptibility to infection and transient myeloproliferative dis...

A case of Niemann-Pick disease type C with neonatal liver failure initially diagnosed a...
https://doi.org/10.1016/j.braindev.2019.01.004
Brain & Development; Kumagai T, Terashima H et. al.

Feb 9th, 2019 - Niemann-Pick type C (NPC) is a lysosomal lipid storage disease with mutation of NPC1/NPC2 genes, which transport lipids in the endosome and lysosome, and various neurological symptoms. NPC patients also develop hepatosplenomegaly or liver disorder...

see more →