- A Case Report of Pseudopseudohypoparathyroidism
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Yim MJ, Jeon JH, Ahn GB, Chung CS, Wie BA
- KMID: 1957570
- J Korean Neurol Assoc.
- 1987 Dec;5(2):283-288.
A case of pseudopseudohypoparathyroidism is reported. The patient, a 23-year-old man, has suffered from generalized tonic-clonic seizure for 16 years and gait disturbance for 4 years. He has the phenotypic... -
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- Two Cases of Albright's Hereditary Osteodystrophy Occurring in Pseudopseudohypoparathyroidism
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Won JH, Hyun DN, Park JS, Chung H, Jung ED
- KMID: 2425023
- Korean J Dermatol.
- 2009 Jul;47(7):820-824.
A 36 year-old man and his 6 month-old daughter presented with multiple, slightly depressed, skin-colored, hard nodules and plaques on the abdomen, back, and both extremities. They also showed abnormal... -
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- A Case of Benign Intracranial Hypertension in Pseudopseudohypoparathyroidism
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Jung WY, Kang SJ, Bae HY
- KMID: 1812904
- J Korean Neurol Assoc.
- 1999 May;17(3):431-434.
We describe a rare case of pseudopseudohypoparathyroidism (PPHP) with benign intracranial hypertension (BIH). A 16 year-old male presented with headache, vomiting, ocular pain, blurred vision, and diplopia following minor head... -
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- Osteoma Cutis as the Presenting Feature of Albright Hereditary Osteodystrophy Associated with Pseudopseudohypoparathyroidism
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Jeong KH, Lew BL, Sim WY
- KMID: 2219385
- Ann Dermatol.
- 2009 May;21(2):154-158.
- doi: 10.5021/ad.2009.21.2.154
Primary osteoma cutis is characterized by the formation of normal bone tissue in the dermis or subcutis without any underlying tissue abnormality or pre-existing calcification. This illness is associated with... -
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- A Case of Pseudopseudohypoparathyroidism with Partial Empty Sella
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Koh JH, Lee Y, Choi JW, Hong TW, Kim MJ, Shin YG, Chung CH
- KMID: 2200532
- J Korean Soc Endocrinol.
- 2004 Aug;19(4):433-438.
Pseudohypoparathyroidism (PHP) is a rare endocrine syndrome, which is characterized by Albright's hereditary osteodystrophy (AHO). Pseudopseudohypoparathyroidism (PPHP) presents with AHO features, but does not show clinical symptoms or the same... -
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- A Case of Pseudopseudohypoparathyroidism with Normal Stature
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Kim SR, Doh YJ, Kim HK, Moon SS, Lee JY, Jeon JH, Kim SW, Kim BW, Lee IK, Kim JG
- KMID: 1468510
- J Korean Endocr Soc.
- 2009 Jun;24(2):138-143.
- doi: 10.3803/jkes.2009.24.2.138
Pseudopseudohypoparathyroidism (PPHP) is characterized by the phenotype of Albright hereditary osteodystrophy (AHO) alone without biochemical evidence of multihormone resistance, which is unlike pseudohypoparathyroidism. AHO is associated with characteristic developmental abnormalities... -
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- Pseudo-Pseudohypoparathyroidism: A Case Report
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Ha KI, Chang JK, Hyun C, Kim JH
- KMID: 2460392
- J Korean Orthop Assoc.
- 1978 Jun;13(2):253-256.
- doi: 10.4055/jkoa.1978.13.2.253
One case of Pseudo-Pseudohypoparathyroidism is reported with the characteristic body features such as short stature, round face, metacarpal sign and multiple exostoses. -
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- Novel Mutation in PTHLH Related to Brachydactyly Type E2 Initially Confused with Unclassical Pseudopseudohypoparathyroidism
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Bae J, Choi HS, Park SY, Lee DE, Lee S
- KMID: 2420494
- Endocrinol Metab.
- 2018 Jun;33(2):252-259.
- doi: 10.3803/EnM.2018.33.2.252
BACKGROUND: Autosomal-dominant brachydactyly type E is a congenital abnormality characterized by small hands and feet, which is a consequence of shortened metacarpals and metatarsals. We recently encountered a young gentleman... -
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- A Case of Osteoma Cutis, a Diagnostic Clue for Albright's Hereditary Osteodystrophy
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Ryu DJ, Oh SH, Han EC, Bae BG, Lee JH
- KMID: 2247921
- Korean J Dermatol.
- 2009 Apr;47(4):435-438.
Albright's hereditary osteodystrophy (AHO) has a broad spectrum of physical findings, including short stature, flattened nasal bridge, round facies, obesity, skeletal anomalies of the hands with brachydactyly, osteoma cutis, mental... -
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- A Case of Cutaneous Ossification occurring in Pseudohypoparathyroidism
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Ahn H, Kim KS, Kim IH, Song HJ, Cheon HW, Lee JW, Oh CH
- KMID: 2383037
- Ann Dermatol.
- 1999 Oct;11(4):263-266.
- doi: 10.5021/ad.1999.11.4.263
In Albright's hereditary osteodystrophy (AHO) including the syndromes of pseudohypoparathyroidism (PHP) and pseudopseudohypoparathyroidism (PPHP), multiple areas of intracutaneous ossification are often encountered. The characteristic features are short stature, round face,... -
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- Polyglandular Autoimmune Syndrome Type III with Primary Hypoparathyroidism
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Kim SJ, Kim SY, Kim HB, Chang H, Cho HC
- KMID: 1973830
- Endocrinol Metab.
- 2013 Sep;28(3):236-240.
- doi: 10.3803/EnM.2013.28.3.236
Polyglandular autoimmune syndrome is defined as multiple endocrine gland insufficiencies accompanied by autoimmune diseases of the endocrine and nonendocrine system. After Schmidt introduced a case of nontuberculosis adrenal gland dysfunction... -
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- Osteoma cutis in Albright's Hereditary Osteodystrophy
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Jung JN, Cho YH, Seo JH, Kim DH, Chung KY
- KMID: 2086815
- Korean J Dermatol.
- 2004 Apr;42(4):493-495.
Albright's hereditary osteodystrophy is an inherited syndrome that encompasses endocrinologic anomaly of pseudohypoparathyroidim or less commonly, pseudo-pseudohypoparathyroidism and various physical stigmata such as mental retardation, short stature, skeletal anomaly of... -
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