Clinical findings include enlarged, abnormally shaped liver and portal hypertension resulting in splenomegaly, hypersplenism, and gastroesophageal varices. [centogene.com]

[…] impairment Rare Symptoms - Less than 30% cases Tics Male infertility Retinal dystrophy Visual loss Microcephaly Hearing impairment Abdominal pain Nyctalopia External genital hypoplasia Vomiting Global developmental delay Clumsiness Growth delay Neoplasm Pain Splenomegaly [mendelian.co]

(For presentation in adulthood, see Male Hypogonadism : Symptoms and Signs .) [msdmanuals.com]

In 1929, he described a 29-year-old female with ichthyosis, hypogonadism, partial gigantism, and diabetes mellitus. [7] [8] References [ edit ] a b "OMIM Entry - 308200 - ICHTHYOSIS AND MALE HYPOGONADISM". www.omim.org. Retrieved 2017-10-29. [en.wikipedia.org]

Laron syndrome Laurence-Moon syndrome leukocyte adhesion deficiency Leukoencephalomyelopathy Leukoencephalopathy with Ataxia Leukomelanoderma, Infantilism, Mental Retardation, Hypodontia, Hypotrichosis Lubinsky Syndrome Male Hypogonadism with Mental Retardation [rgd.mcw.edu]

[…] non descent of the testicle urethral opening on the inferior side of the penis urethral opening on the superior side of the penis -a decrease in either of two major functions in the testes: 1) sperm production, or 2) testosterone production Male hypogonadism [quizlet.com]

MORPHOLOGY OF THE PITUITARY 19 THE OPTIC CHIASM IN ENDOCRINOLOGIC 204 PARANEOPLASTIC ENDOCRINE 223 SEX HORMONES AND HUMAN 219 APPROACH TO THE PATIENT WITH 37 ADVERSE EFFECTS OF IODIDE 360 MORPHOLOGY OF THE THYROID 38 NONTOXIC GOITER 366 SYNTHESIS AND [books.google.es]

Goiter, multinodular 1, with or with out sertoli-leydig cell tum or s Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Goiter, multinodular 1, with or with out sertoli-leydig cell tum or s phenotype from the curated ClinVar [amp.pharm.mssm.edu]

Familial, with Hypothyroidism Goiter, Nonendemic Simple Gout, HPRT-related GRACILE Syndrome Greater Agonists Promoted Contractility Greig Cephalopolysyndactyly Syndrome Griscelli Syndrome, Type 2 Growth Hormone Deficiency Growth Hormone Deficiency, [sequencing.com]

Non-autoimmune diabetes mellitus, thyroid dysfunction and/or goiter and sometimes hypoparathyroidism should steer the diagnosis towards a respiratory chain defect. [ojrd.biomedcentral.com]

MORPHOLOGY OF THE PITUITARY 19 THE OPTIC CHIASM IN ENDOCRINOLOGIC 204 PARANEOPLASTIC ENDOCRINE 223 SEX HORMONES AND HUMAN 219 APPROACH TO THE PATIENT WITH 37 ADVERSE EFFECTS OF IODIDE 360 MORPHOLOGY OF THE THYROID 38 NONTOXIC GOITER 366 SYNTHESIS AND 39 THE THYROID [books.google.es]

The disorder is characterized by bruising, fatigue, anemia, low blood platelet count and enlargement of the liver and spleen, and is caused by a hereditary deficiency of the enzyme glucocerebrosidase (also known as … Previous 1 2 3 4 ... 7 Next Last [checkrare.com]

With low levels of thyroid stimulating hormone, people will experience many different symptoms: fatigue, sensitivity to cold, poor ability to concentrate, weight gain, constipation, shortness of breath. [rarediseases.org]

[…] painless testicular mass, or as a testicular swelling with vague discomfort, suggesting a mild epididymitis, though there will be no response to antibiotics Staging germ cell tumors? Stage I limited to the testis, epididymis, or spermatic cord. [quizlet.com]

With low levels of thyroid stimulating hormone, people will experience many different symptoms: fatigue, sensitivity to cold, poor ability to concentrate, weight gain, constipation, shortness of breath. [rarediseases.org]

Tics Male infertility Retinal dystrophy Visual loss Microcephaly Hearing impairment Abdominal pain Nyctalopia External genital hypoplasia Vomiting Global developmental delay Clumsiness Growth delay Neoplasm Pain Splenomegaly Fever Blindness Seizures Constipation [mendelian.co]

catecholaminergic polymorphic, 2 CASQ2 Ventricular tachycardia, catecholaminergic polymorphic, 5, with or without muscle weakness, 615441 TRDN VLCAD deficiency ACADVL Walker-Warburg syndrome (congenital with brain and eye anomalies) FKTN Wilson disease [ceifer.com]

VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1, WITH OR WITHOUT ATRIAL DYSFUNCTION AND/OR DILATED CARDIOMYOPATHY Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC [amp.pharm.mssm.edu]

[…] limb-girdle, type 2A) CARD9 (Candidiasis, familial chronic mucocutaneous, autosomal recessive) CASK (FG syndrome 4) CASP10 (Autoimmune lymphoproliferative syndrome, type II) CASP8 (Autoimmune lymphoproliferative syndrome, type IIB) CASQ2 (Ventricular tachycardia [en.praenatal-medizin.de]

Updated clinical guidelines for diabetes, lipid disorders, obesity management, osteoporosis, and more, as well as essential treatment updates for the medical management of acromegaly, Cushing's Disease, hypercalcemia, and diabetes mellitus. [books.google.com]

100%) HP:0000510 3 pigmentary retinopathy 60 33 obligate (100%) Obligate (100%) HP:0000580 4 delayed skeletal maturation 60 33 hallmark (90%) Very frequent (99-80%) HP:0002750 5 delayed puberty 60 33 hallmark (90%) Very frequent (99-80%) HP:0000823 6 osteoporosis [malacards.org]

Screening for primary or hypogonadotrophic hypogonadism, as well as osteoporosis, should be done in adulthood. [ojrd.biomedcentral.com]

ATAXIA AND SEIZURES Nijmegen breakage syndrome nonphotosensitive trichothiodystrophy oculocutaneous albinism Oligodontia-Colorectal Cancer Syndrome Optic Atrophy 10 with or without Ataxia, Mental Retardation, and Seizures orofaciodigital syndrome V osteoporosis-pseudoglioma [rgd.mcw.edu]

Osteogenesis imperfecta, type XIX; Olmsted syndrome, X-linked; IFAP syndrome with or without BRESHECK syndrome; Keratosis follicularis spinulosa decalvans, X-linked P3H1 Osteogenesis imperfecta, type VIII PLOD2 Bruck syndrome 2 PLS3 Bone mineral density QTL18, osteoporosis [asperbio.com]

[…] hallmark (90%) HP:0003164 15 obesity 60 33 frequent (33%) Frequent (79-30%) HP:0001513 16 abnormality of the dentition 60 33 frequent (33%) Frequent (79-30%) HP:0000164 17 short stature 60 33 frequent (33%) Frequent (79-30%) HP:0004322 18 recurrent fractures [malacards.org]

Gene Set From OMIM Gene-Disease Associations genes associated with the spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or with out fractures phenotype from the curated OMIM Gene-Disease Associations dataset. sh or t-rib th or acic dysplasia [amp.pharm.mssm.edu]

Spinal muscular atrophy, distal, X-linked 3 ATP6V0A2 Cutis laxa, autosomal recessive, type IIA; Wrinkly skin syndrome B3GALT6 Ehlers-Danlos syndrome, spondylodysplastic type, 2; Spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures [asperbio.com]

Type 1 hyperoxaluria is also associated with advanced skeletal age in young patients, increased FGF23 (Fibroblast Growth Factor 23) levels and decreased bone mineral density, thus promoting fractures [ 132 ]. [ojrd.biomedcentral.com]

fractures 60 33 frequent (33%) Frequent (79-30%) HP:0002757 19 reduced bone mineral density 60 Frequent (79-30%) 20 anterior hypopituitarism 60 Very frequent (99-80%) 21 hypothalamic gonadotropin-releasing hormone (gnrh) deficiency 60 Very frequent [malacards.org]

[…] septal defect Abnormal cardiac septum morphology Nephrotic syndrome Abnormal cornea morphology Absent frontal sinuses Crackles Abnormal respiratory motile cilium morphology Scoliosis Hepatomegaly Diarrhea Erythema Hyperhidrosis Arthritis Arthralgia Myalgia [mendelian.co]

Symptoms of metachromatic leukodystrophy may include seizures, personality changes, spasticity, progressive dementia, painful paresthesias, motor disturbances progressing to paralysis, and/or visual impairment leading to blindness. [rarediseases.org]

Services Research Training Industry About us Home Ontologies Documentation About Contact Us OLS Orphanet Rare Disease Ontolog ORDO Orphanet:2235 This syndrome is characterized by the association of hypogonadotropic hypogonadism (with primary amenorrhea [ebi.ac.uk]

HP:0000580 4 delayed skeletal maturation 60 33 hallmark (90%) Very frequent (99-80%) HP:0002750 5 delayed puberty 60 33 hallmark (90%) Very frequent (99-80%) HP:0000823 6 osteoporosis 60 33 hallmark (90%) Very frequent (99-80%) HP:0000939 7 primary amenorrhea [malacards.org]

The young woman, aged 18 years, had secondary amenorrhea and polycystic ovaries; her brother, aged 15 years, had gynecomastia and hypergonadotropic hypogonadism. [omim.org]

The females presented with primary amenorrhea. Both had partial alopecia especially on the temporo-parietal regions of the cranium. Their eyebrows and eyelashes were intact. They had streak ovaries. [jpma.org.pk]

Bronchitis Immotile cilia Ciliary dyskinesia Recurrent otitis media Otitis media Leukocytosis Dyskinesia Respiratory tract infection Pneumonia Recurrent respiratory infections Primary amenorrhea Schwannoma Pterygium Multiple lentigines Asymmetry of the [mendelian.co]

Services Research Training Industry About us Home Ontologies Documentation About Contact Us OLS Orphanet Rare Disease Ontolog ORDO Orphanet:2235 This syndrome is characterized by the association of hypogonadotropic hypogonadism (with primary amenorrhea [ebi.ac.uk]

amenorrhea 60 33 hallmark (90%) Very frequent (99-80%) HP:0000786 8 absence of secondary sex characteristics 60 33 hallmark (90%) Very frequent (99-80%) HP:0008187 9 decreased fertility 60 33 hallmark (90%) Very frequent (99-80%) HP:0000144 10 secondary [malacards.org]

The females presented with primary amenorrhea. Both had partial alopecia especially on the temporo-parietal regions of the cranium. Their eyebrows and eyelashes were intact. They had streak ovaries. [jpma.org.pk]

The initial findings include one or several of the following features: gait disturbance, visual impairment due to chorioretinal dystrophy or atrophy, anterior hypopituitarism, or delayed puberty/primary amenorrhea. [ncbi.nlm.nih.gov]

amenorrhea Schwannoma Pterygium Multiple lentigines Asymmetry of the thorax Synovitis Abnormality of color vision Atrial flutter Restrictive cardiomyopathy Neuroblastoma Abnormality of blood and blood-forming tissues Abnormality of the vertebral column [mendelian.co]

Brand-new chapters and comprehensive updates throughout include new information on perioperative care in adults and children, premature ejaculation, retroperitoneal tumors, nocturia, and more! [books.google.com]

Brand-new chapters and comprehensive updates throughout include new information on perioperative care in adults and children, premature ejaculation, retroperitoneal tumors, nocturia, and more! [books.google.com]

bone age due to thyroid hormone metabolism deficiency Short stature-pituitary and cerebellar defects-small sella turcica syndrome Sickle cell anemia Siegler-Brewer-Carey syndrome Staphylococcal necrotizing pneumonia Sudden infant death-dysgenesis of [se-atlas.de]

THYROID FUNCTION TEST 47 THYROID DISORDERS OF INFANCY 462 P A RT IV CALCIUM AND BONE METABOLISM 473 MORPHOLOGY OF THE PARATHYROID 51 PARATHYROID HORMONE 497 PHYSIOLOGY OF CALCIUM 52 PARATHYROID HORMONERELATED 512 CLINICAL APPLICATION OF BONE MINERAL [books.google.es]