Cover Image

Congenital amegakaryocytic thrombocytopenia- A rare case report

Saved in:

Bibliographic Details
Main Authors:	Ariba Afeeh (Author), Vikas Mahajan (Author), Ravinder K. Gupta (Author)
Format:	Book
Published:	Elsevier, 2024-01-01T00:00:00Z.
Subjects:	article
Online Access:	Connect to this object online.
Tags:	Add Tag No Tags, Be the first to tag this record!

Similar Items

Congenital Amegakaryocytic Thrombocytopenia: A Brief Review of the Literature
by: Fatma S. Al-Qahtani
Published: (2010)

Transient acquired amegakaryocytic thrombocytopenia associated with Pediatric Hodgkin Lymphoma: A case report
by: Fatima Meraj, et al.
Published: (2021)

Myelodysplastic Syndrome Presenting as Amegakaryocytic Thrombocytopenia in a Collodion Baby
by: Mohammed Al Pakra MD, et al.
Published: (2015)

Hard to find and tricky to treat: A case series of acquired amegakaryocytic thrombocytopenia
by: Amina Anwar, et al.
Published: (2023)

Haematological profile in neonates - A hospital-based study
by: Ariba Afeeh, et al.
Published: (2024)

Case Report: Successful Avatrombopag Treatment for Two Cases of Anti-PD-1 Antibody-Induced Acquired Amegakaryocytic Thrombocytopenia
by: Xiaofang Tu, et al.
Published: (2022)

A novel missense mutation in the MECOM gene in a Chinese boy with radioulnar synostosis with amegakaryocytic thrombocytopenia
by: Duowen Huang, et al.
Published: (2024)

Non-myeloablative conditioning is sufficient to achieve complete donor myeloid chimerism following matched sibling donor bone marrow transplant for myeloproliferative leukemia virus oncogene (MPL) mutation-driven congenital amegakaryocytic thrombocytopenia: Case report
by: Joseph Hai Oved, et al.
Published: (2022)

Unusual yet isolated oral manifestations of persistent thrombocytopenia - A rare case report
by: Amit Byatnal, et al.
Published: (2015)

A rare case of eptifibatide-induced thrombocytopenia
by: Khalil Kamar, et al.
Published: (2021)

Severe congenital thrombocytopenia and platelet dysfunction due to novel WAS gene mutation: case report
by: Darjan Kardum, et al.
Published: (2022)

Foetal and neonatal alloimune thrombocytopenia as a rare exapmle of thrombocytopenia in newborn
by: Maciej Kamiński, et al.
Published: (2018)

Foetal and neonatal alloimune thrombocytopenia as a rare exapmle of thrombocytopenia in newborn
by: Maciej Kamiński, et al.
Published: (2018)

Congenital thrombocytopenia associated with GNE mutations in twin sisters: a case report and literature review
by: Xin Li, et al.
Published: (2020)

Mucocutaneous Manifestations in a Case of Immune Thrombocytopenia: Reporting a Rare Presentation with Dermoscopic Findings
by: Preema Sinha, et al.
Published: (2024)

Congenital epulides: A rare case report
by: Saurabh Kumar, et al.
Published: (2014)

GCSF induced thrombocytopenia - A rare find
by: Juhi Mehrotra, et al.
Published: (2022)

Isolated thrombocytopenia report of a rare presentation of childhood Systemic Lupus Erythematosus
by: Ahmad Tamaddoni, et al.
Published: (2015)

Unilateral Acute Parotitis: A Novel Manifestation of Pediatric Coronavirus Disease
by: Sushil Sharma, et al.
Published: (2022)

A rare case report of congenital granular cell epulis
by: K R Vijayalakshmi, et al.
Published: (2021)

Immune thrombocytopenia, Strongyloides stercoralis hyperinfection syndrome with coinfection of Cryptosporidium: A rare case
by: Jitu M Kalita, et al.
Published: (2021)

Pattern and Clinical Profile of Congenital Heart Disease in a Teaching Hospital
by: Ravinder K. Gupta, et al.
Published: (2021)

Sirenomelia- A rare congenital anomaly: Case report
by: Dipanjali Thombare, et al.
Published: (2023)

Hepatoid adenocarcinoma of stomach: Case report of a rare histological variant
by: Vidisha Mahajan, et al.
Published: (2014)

Osteopetrosis Presenting with Neonatal Thrombocytopenia: A Case Report
by: Mohammad Kazemian, et al.
Published: (2018)

Nasopharyngeal carcinoma presenting as muscular atrophy - A rare case report and role of oral physician
by: Ravinder Singh, et al.
Published: (2019)

Vancomycin-Induced Thrombocytopenia as a Less Considered Contributing Cause in Differential Diagnosis of Thrombocytopenia: A Case Report
by: Sholeh Ebrahimpour, et al.
Published: (2019)

Missing Cells - A Rare Case of Persisting Thrombocytopenia in Pregnancy With Dengue and Role of Romiplostim in These Cases
by: Ruchita Sinha, et al.
Published: (2023)

Congenital Rubella Syndrome as a possible cause for persistent thrombocytopenia in early infancy: The Forgotten Culprit
by: Jogender Kumar, et al.
Published: (2022)

Unravelling the unique case of congenital infiltrating lipomatosis of face with its rare associations-A case report
by: Ramandeep Singh, et al.
Published: (2024)

Congenital upper lip pit: A rare case report
by: Leena James, et al.
Published: (2015)

Congenital double-double lip: A rare case report
by: Swati Phore, et al.
Published: (2017)

Congenital insensitivity to pain: Case report of a rare entity
by: Swati Dahiya, et al.
Published: (2018)

Refractory thrombocytopenia could be a rare initial presentation of Noonan syndrome in newborn infants: a case report and literature review
by: Xiujun Tang, et al.
Published: (2022)

Heparin-induced thrombocytopenia: a rare presentation with skin necrosis
by: Filipa David, et al.
Published: (2023)

Littoral cell angioma: A rare cause of pediatric thrombocytopenia
by: Mitul Jasani, et al.
Published: (2018)

Evans syndrome: A rare cause of persistent thrombocytopenia in children
by: Kanchan Channawar, et al.
Published: (2015)

Tirofiban Induced Thrombocytopenia: A Rare but Severe Adverse Effect
by: Muhammad Shabbir Rawala, et al.
Published: (2020)

Congenital extraskeletal Ewing's sarcoma of chest wall - A rare case report
by: Bhagyalakshmi Atla, et al.
Published: (2011)

A rare case of metastatic small cell neuroendocrine carcinoma of the lung presenting as isolated thrombocytopenia
by: Adreana DeMarinis, et al.
Published: (2019)