Early Onset of Severe Anemia Caused by Hb Calgary (HBB: C.194G > T): Another Case Report
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作者:
Jiang, Hua
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Guangzhou Med Univ, Guangzhou Women & Childrens Med Ctr, Dept Hematol Oncol, Guangzhou, Guangdong, Peoples R ChinaGuangzhou Med Univ, Guangzhou Women & Childrens Med Ctr, Dept Hematol Oncol, Guangzhou, Guangdong, Peoples R China
Jiang, Hua
[1
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Li, Dong-Zhi
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Guangzhou Med Univ, Prenatal Diagnost Ctr, Guangzhou Women & Childrens Med Ctr, Jinsui Rd 9, Guangzhou, Guangdong, Peoples R ChinaGuangzhou Med Univ, Guangzhou Women & Childrens Med Ctr, Dept Hematol Oncol, Guangzhou, Guangdong, Peoples R China
Li, Dong-Zhi
[2
]
机构:
[1] Guangzhou Med Univ, Guangzhou Women & Childrens Med Ctr, Dept Hematol Oncol, Guangzhou, Guangdong, Peoples R China
[2] Guangzhou Med Univ, Prenatal Diagnost Ctr, Guangzhou Women & Childrens Med Ctr, Jinsui Rd 9, Guangzhou, Guangdong, Peoples R China
Unstable hemoglobin (Hb) variants are a rare cause of congenital hemolytic anemia. We describe a Chinese girl who presented with transfusion-dependent anemia in early infancy. Her diagnosis of Hb Calgary [beta 64(E8)Gly > Val; HBB:c.194G > T] was not made until molecular testing was performed at the age of 5 years. Our case highlights the importance of early genetic testing in order to make the diagnosis, which may not only be useful for patient management and family counseling, but also for avoiding further unnecessary investigative attempts.
机构:
Yokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa 232, JapanYokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa 232, Japan
Miyatake, S.
Miyake, N.
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Yokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa 232, JapanYokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa 232, Japan
Miyake, N.
Touho, H.
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Touho Neurosurg Clin, Osaka, JapanYokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa 232, Japan
Touho, H.
Nishimura-Tadaki, A.
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Yokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa 232, JapanYokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa 232, Japan
Nishimura-Tadaki, A.
Kondo, Y.
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Yokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa 232, JapanYokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa 232, Japan
Kondo, Y.
Okada, I.
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Yokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa 232, JapanYokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa 232, Japan
Okada, I.
Tsurusaki, Y.
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Yokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa 232, JapanYokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa 232, Japan
Tsurusaki, Y.
Doi, H.
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Yokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa 232, JapanYokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa 232, Japan
Doi, H.
Sakai, H.
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Yokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa 232, JapanYokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa 232, Japan
Sakai, H.
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Saitsu, H.
Shimojima, K.
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Tokyo Womens Med Univ, Inst Integrated Med Sci, Tokyo, JapanYokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa 232, Japan
Shimojima, K.
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Yamamoto, T.
Higurashi, M.
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Yokohama City Univ, Grad Sch Med, Dept Neurosurg, Yokohama, Kanagawa 232, JapanYokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa 232, Japan
Higurashi, M.
Kawahara, N.
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Yokohama City Univ, Grad Sch Med, Dept Neurosurg, Yokohama, Kanagawa 232, JapanYokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa 232, Japan
Kawahara, N.
Kawauchi, H.
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机构:
Tone Chuo Hosp, Dept Neurosurg, Gunma, JapanYokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa 232, Japan
Kawauchi, H.
Nagasaka, K.
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机构:
Tone Chuo Hosp, Dept Neurosurg, Gunma, JapanYokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa 232, Japan
Nagasaka, K.
Okamoto, N.
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Osaka Med Ctr, Div Med Genet, Osaka, JapanYokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa 232, Japan
Okamoto, N.
Mori, T.
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Ichikawa City Rehabil Hosp, Dept Rehabil Med, Ichikawa, JapanYokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa 232, Japan
Mori, T.
Koyano, S.
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Yokohama City Univ, Grad Sch Med, Dept Clin Neurol & Stroke Med, Yokohama, Kanagawa 232, JapanYokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa 232, Japan
Koyano, S.
Kuroiwa, Y.
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Yokohama City Univ, Grad Sch Med, Dept Clin Neurol & Stroke Med, Yokohama, Kanagawa 232, JapanYokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa 232, Japan
Kuroiwa, Y.
Taguri, M.
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Yokohama City Univ, Med Ctr, Dept Biostat & Epidemiol, Yokohama, Kanagawa 232, JapanYokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa 232, Japan
Taguri, M.
Morita, S.
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Yokohama City Univ, Med Ctr, Dept Biostat & Epidemiol, Yokohama, Kanagawa 232, JapanYokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa 232, Japan
Morita, S.
Matsubara, Y.
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机构:
Tohoku Univ, Sch Med, Dept Med Genet, Sendai, Miyagi 980, JapanYokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa 232, Japan
Matsubara, Y.
Kure, S.
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机构:
Tohoku Univ, Sch Med, Dept Pediat, Sendai, Miyagi 980, JapanYokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa 232, Japan
Kure, S.
Matsumoto, N.
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Yokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa 232, JapanYokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa 232, Japan
机构:
St Etienne Univ Hosp, Neonatal Pediat Care Unit, St Etienne, FranceLa Timone Childrens Hosp, APHM, Pediat Oncohematol Dept, Reference Ctr Rare Red Cell Disorders, Marseille, France